시장보고서
상품코드
1788268

세계의 의약품 불순물 합성 및 분리 서비스 시장

Pharmaceutical Impurity Synthesis and Isolation Services

발행일: | 리서치사: Market Glass, Inc. (Formerly Global Industry Analysts, Inc.) | 페이지 정보: 영문 245 Pages | 배송안내 : 1-2일 (영업일 기준)

    
    
    



※ 본 상품은 영문 자료로 한글과 영문 목차에 불일치하는 내용이 있을 경우 영문을 우선합니다. 정확한 검토를 위해 영문 목차를 참고해주시기 바랍니다.

세계의 의약품 불순물 합성 및 분리 서비스 시장은 2030년까지 21억 달러에 도달

2024년에 13억 달러로 추정되는 세계의 의약품 불순물 합성 및 분리 서비스 시장은 2024-2030년에 CAGR 7.7%로 성장하며, 2030년에는 21억 달러에 달할 것으로 예측됩니다. 이 리포트에서 분석한 부문의 하나인 분리 서비스는 CAGR 8.9%를 기록하며, 분석 기간 종료시에는 13억 달러에 달할 것으로 예측됩니다. 분석 서비스 분야의 성장률은 분석 기간에 CAGR 5.7%로 추정됩니다.

미국 시장은 3억 4,630만 달러로 추정, 중국은 CAGR 7.5%로 성장 예측

미국의 의약품 불순물 합성 및 분리 서비스 시장은 2024년에 3억 4,630만 달러로 추정됩니다. 세계 2위의 경제대국인 중국은 분석 기간인 2024-2030년의 CAGR을 7.5%로, 2030년까지 3억 2,890만 달러의 시장 규모에 달할 것으로 예측됩니다. 기타 주목할 만한 지역별 시장으로는 일본과 캐나다가 있으며, 분석 기간 중 CAGR은 각각 7.3%와 6.4%로 예측됩니다. 유럽에서는 독일이 CAGR 약 6.1%로 성장할 것으로 예측됩니다.

의약품 제조 장비-주요 동향과 촉진요인 정리

의약품 제조 장비가 의약품 제조를 어떻게 변화시킬 것인가?

의약품 제조 장비는 정제, 캡슐제, 주사제, 생물제제 등의 의약품을 효율적이고 정확하며 고품질로 제조하는 데 있으며, 매우 중요한 역할을 합니다. 업계가 자동화, 공정 최적화, 엄격한 규제 표준을 도입함에 따라 제조 기술의 발전은 의약품 제조 공정을 재구성하고 있습니다. 최신 제약 장비는 제품의 일관성을 높이고, 확장성을 향상시키며, 인적 오류를 줄이면서 GMP(Good Manufacturing Practice) 및 미국 FDA, EMA, WHO 등의 규제 요건을 준수할 수 있도록 설계되어 있습니다.

의약품 제조의 중요한 측면은 특히 무균 제제 및 주사제 제조에서 무균 및 오염 제어를 보장하는 것입니다. 고속 충전 라인, 아이솔레이터, 클린 인 플레이스(CIP) 시스템은 최신 제조 공장의 필수적인 요소입니다. 또한 연속 생산(CM)은 실시간 모니터링과 효율성 향상을 위해 기존의 일괄 처리보다 더 많은 지지를 받고 있습니다. 사물인터넷(IoT), 인공지능(AI) 등 인더스트리 4.0 기술의 통합은 공정 자동화, 예지보전, 품질관리를 더욱 강화하여 의약품 공급망 전반의 효율성을 높이고 있습니다.

의약품 제조 장비의 진화를 촉진하는 시장 동향은?

제약 제조 장비 시장은 업계의 진화하는 요구에 부응하는 새로운 동향에 따라 빠르게 변화하고 있습니다. 가장 중요한 동향 중 하나는 특히 생물제제 제조에서 일회용 기술(SUT)의 부상입니다. 일회용 바이오리액터, 여과 시스템, 일회용 튜브는 오염 위험을 줄이고, 유연성을 높이며, 운영 비용을 낮추기 때문에 기존의 스테인리스강 장비를 대체할 수 있는 매력적인 대안이 되고 있습니다. 이러한 변화는 맞춤형 의료와 세포 및 유전자 치료에 집중하는 개발 및 제조수탁기관(CDMO)과 생명공학 기업에게 특히 유리합니다.

또 다른 주요 동향은 배치 생산보다 연속 생산(CM)의 채택이 확대되고 있다는 점입니다. CM은 실시간 품질 보증을 가능하게 하고, 제조 시간을 단축하고, 낭비를 최소화함으로써 의약품 제조에 대한 보다 효율적이고 통제된 접근 방식을 제공합니다. FDA와 같은 규제기관은 의약품의 품질과 공급망의 강인성을 향상시키기 위해 CM의 채택을 적극적으로 장려하고 있습니다. 또한 3D 프린팅 기술은 개인화된 약물 제형과 복잡한 제형 제조를 가능하게 함으로써 의약품 제조에 혁명을 일으켜 환자 치료 결과를 개선할 수 있습니다.

또한 고역가 활성 의약품 성분(HPAPI)에 대한 수요 증가는 봉쇄 및 격리 기술의 발전을 촉진하고 있습니다. 제약회사들이 암 치료제, 호르몬 기반 치료제 등 보다 강력한 화합물을 취급함에 따라 고농도 봉쇄 글러브 박스, 폐쇄형 이송 장치(CSTD) 등 특수 장비에 대한 수요가 급증하고 있습니다. 지속가능성과 에너지 효율이 높은 장비에 대한 관심도 높아지고 있으며, 제조업체들은 탄소발자국과 자원 소비를 최소화하는 친환경 생산 시스템에 투자하고 있습니다.

최종 용도는 의약품 제조 장비 수요에 어떤 영향을 미치고 있는가?

의약품 제조 장비에 대한 수요는 경구용 고형제(OSD), 비경구용 의약품, 바이오의약품, 특수 의약품 등 의약품 제조 부문의 다양한 용도와 밀접한 관련이 있습니다. 정제 및 캡슐을 포함한 OSD 부문은 여전히 제조 장비의 가장 큰 소비자이며, 정밀도와 일관성을 보장하기 위해 고급 정제 프레스기, 과립기, 코팅기를 필요로 합니다. 또한 엄격한 품질관리 기준을 유지하면서 생산 효율을 높이고자 하는 제조업체의 경우, 고속 인캡슐레이션 장비에 대한 수요도 증가하고 있습니다.

주사제 및 바이오의약품 분야에서는 생물제제, 백신, 유전자 치료제의 생산이 확대됨에 따라 무균 처리 장비에 대한 수요가 급증하고 있습니다. 여기에는 첨단 충진 마감 시스템, 동결 건조 기술, 생산 공정 전반에 걸쳐 무균 상태를 유지하는 아이솔레이터 등이 포함됩니다. 맞춤형 의료와 소량 생산되는 생물제제 증가로 다양한 생산 규모에 대응할 수 있는 유연한 모듈식 제조 장비에 대한 요구가 더욱 커지고 있습니다.

첨단 포장 분야에서도 기술 발전이 두드러지게 나타나고 있습니다. 위조 방지 기술 및 추적 시스템과 같은 스마트 패키징 솔루션은 의약품 제조에 필수적인 요소로 자리 잡고 있습니다. 직렬화 및 집계 장비는 의약품 공급망 보안법(DSCSA) 및 위조 의약품 지침(FMD)과 같이 공급망 전반에 걸쳐 의약품을 엄격하게 추적해야 하는 세계 규제 준수를 보장하는 데 중요한 요소입니다. 를 준수하도록 하는 중요한 컴포넌트입니다.

의약품 제조 장비 시장의 성장 동력은 무엇인가?

제약 제조 장비 시장의 성장은 자동화 수요 증가, 생물제제 생산량 증가, 규제 요건 변화 등 여러 요인에 의해 주도되고 있습니다. 연속 처리, 디지털 트윈 시뮬레이션, 로봇 공학 등 첨단 제조 기술로의 전환은 생산 효율을 높이고 운영 비용을 절감하고 있습니다. AI를 활용한 예지보전과 실시간 공정 분석을 통해 설비 가동률을 더욱 최적화하고 다운타임을 최소화하며 전반적인 생산성을 향상시키고 있습니다.

기업은 모노클로널 항체, mRNA 기반 치료, 맞춤형 의료에 대한 수요 증가에 대응하기 위해 최첨단 바이오프로세스 장비에 많은 투자를 하고 있습니다. 또한 제약업계는 지속가능성과 친환경 제조에 중점을 두고 있으며, 세계 환경 기준에 부합하는 에너지 효율이 높은 장비와 폐기물 감소 기술에 대한 투자를 촉진하고 있습니다.

혁신적인 제조 기술, 특히 연속 생산 및 실시간 품질관리에 대한 규제 당국의 지원도 시장 성장을 가속화하고 있습니다. FDA와 EMA와 같은 기관은 제약회사들이 의약품의 품질을 보장하고 제조의 비효율성을 줄이기 위해 첨단 처리 장비를 채택하도록 촉구하고 있습니다. 또한 CDMO 및 수탁제조 서비스의 확대로 인해 다양한 제형과 다양한 생산량에 대응할 수 있는 유연하고 확장 가능한 제조 장비에 대한 수요가 증가하고 있습니다.

제약 산업이 계속 발전함에 따라 첨단 제조 장비에 대한 수요는 자동화, 디지털화, 혁신적 가공 기술을 통해 의약품 제조의 미래를 형성할 것입니다.

부문

서비스(분리 서비스, 분석 서비스, 합성 서비스), 불순물(무기 불순물, 유기 불순물, 잔류 용매), 기술(크로마토그래피 기술, 분광 기술, 결정화 기술, 하이프네이트 기술, 기타 기술), 용도(상업 제조 용도, 의약품 개발 용도, 품질관리 용도, 규제 준수 용도), 최종 용도(바이오테크놀러지 및 제약 기업 최종 용도, 계약 연구기관 최종 용도, 기타 최종 용도)

조사 대상 기업의 예

  • Alfa Chemistry
  • Almac Group
  • BOC Sciences
  • Cambrex Corporation
  • Catalent, Inc.
  • Charles River Laboratories
  • Epichem
  • Eurofins Scientific
  • Frontage Laboratories
  • Intertek Group plc
  • Laboratory Corporation of America Holdings(Labcorp)
  • PCI Pharma Services
  • Pharmaron
  • Piramal Pharma Solutions
  • SGS Societe Generale de Surveillance SA
  • Symeres
  • Syngene International Limited
  • Veeda Clinical Research
  • Veeprho
  • WuXi AppTec

AI 통합

Global Industry Analysts는 유효한 전문가 컨텐츠와 AI 툴에 의해 시장 정보와 경쟁 정보를 변혁하고 있습니다.

Global Industry Analysts는 일반적인 LLM나 업계별 SLM 쿼리에 따르는 대신에, 비디오 기록, 블로그, 검색 엔진 조사, 대량 기업, 제품/서비스, 시장 데이터 등, 전 세계 전문가로부터 수집한 컨텐츠 리포지토리를 구축했습니다.

관세 영향 계수

Global Industry Analysts는 본사 소재지, 제조거점, 수출입(완제품 및 OEM)을 기준으로 기업의 경쟁력 변화를 예측했습니다. 이러한 복잡하고 다면적인 시장 역학은 수입원가(COGS) 증가, 수익성 하락, 공급망 재편 등 미시적, 거시적 시장 역학 중에서도 특히 경쟁사들에게 영향을 미칠 것으로 예측됩니다.

목차

제1장 조사 방법

제2장 개요

  • 시장 개요
  • 주요 기업
  • 시장 동향과 촉진요인
  • 세계 시장 전망

제3장 시장 분석

  • 미국
  • 캐나다
  • 일본
  • 중국
  • 유럽
  • 프랑스
  • 독일
  • 이탈리아
  • 영국
  • 기타 유럽
  • 아시아태평양
  • 기타 지역

제4장 경쟁

KSA 25.08.18

Global Pharmaceutical Impurity Synthesis and Isolation Services Market to Reach US$2.1 Billion by 2030

The global market for Pharmaceutical Impurity Synthesis and Isolation Services estimated at US$1.3 Billion in the year 2024, is expected to reach US$2.1 Billion by 2030, growing at a CAGR of 7.7% over the analysis period 2024-2030. Isolation Services, one of the segments analyzed in the report, is expected to record a 8.9% CAGR and reach US$1.3 Billion by the end of the analysis period. Growth in the Analytical Services segment is estimated at 5.7% CAGR over the analysis period.

The U.S. Market is Estimated at US$346.3 Million While China is Forecast to Grow at 7.5% CAGR

The Pharmaceutical Impurity Synthesis and Isolation Services market in the U.S. is estimated at US$346.3 Million in the year 2024. China, the world's second largest economy, is forecast to reach a projected market size of US$328.9 Million by the year 2030 trailing a CAGR of 7.5% over the analysis period 2024-2030. Among the other noteworthy geographic markets are Japan and Canada, each forecast to grow at a CAGR of 7.3% and 6.4% respectively over the analysis period. Within Europe, Germany is forecast to grow at approximately 6.1% CAGR.

Pharmaceutical Manufacturing Equipment- Key Trends & Drivers Summarized

How Is Pharmaceutical Manufacturing Equipment Transforming Drug Production?

Pharmaceutical manufacturing equipment plays a pivotal role in ensuring the efficient, precise, and high-quality production of medications, including tablets, capsules, injectables, and biologics. As the industry embraces automation, process optimization, and stringent regulatory standards, advancements in manufacturing technology are reshaping drug production processes. Modern pharmaceutical equipment is designed to improve product consistency, enhance scalability, and reduce human error while maintaining compliance with Good Manufacturing Practices (GMP) and regulatory requirements set by agencies like the U.S. FDA, EMA, and WHO.

A key aspect of pharmaceutical manufacturing is ensuring sterility and contamination control, particularly for aseptic and injectable drug production. High-speed filling lines, isolators, and clean-in-place (CIP) systems have become essential components of modern manufacturing plants. Additionally, continuous manufacturing (CM) is gaining traction over traditional batch processing, allowing for real-time monitoring and improved efficiency. The integration of Industry 4.0 technologies, such as the Internet of Things (IoT) and artificial intelligence (AI), is further enhancing process automation, predictive maintenance, and quality control, driving efficiency across the pharmaceutical supply chain.

What Market Trends Are Driving the Evolution of Pharmaceutical Manufacturing Equipment?

The pharmaceutical manufacturing equipment market is experiencing rapid transformation due to emerging trends that address the industry's evolving needs. One of the most significant trends is the rise of single-use technology (SUT), particularly in biologics manufacturing. Single-use bioreactors, filtration systems, and disposable tubing reduce contamination risks, enhance flexibility, and lower operational costs, making them an attractive alternative to traditional stainless-steel equipment. This shift is particularly beneficial for contract development and manufacturing organizations (CDMOs) and biotech firms focused on personalized medicine and cell and gene therapies.

Another key trend is the growing adoption of continuous manufacturing (CM) over batch production. CM offers a more efficient and controlled approach to pharmaceutical production by enabling real-time quality assurance, reducing production time, and minimizing waste. Regulatory agencies, including the FDA, have been actively encouraging the adoption of CM to improve drug quality and supply chain resilience. In addition, 3D printing technology is revolutionizing pharmaceutical manufacturing by allowing for the production of personalized drug formulations and complex dosage forms, leading to improved patient outcomes.

Furthermore, the increasing demand for high-potency active pharmaceutical ingredients (HPAPIs) has driven advancements in containment and isolation technology. The need for specialized equipment, such as high-containment glove boxes and closed-system transfer devices (CSTDs), has surged as pharmaceutical manufacturers work with more potent compounds, including oncology drugs and hormone-based treatments. The focus on sustainability and energy-efficient equipment is also rising, with manufacturers investing in eco-friendly production systems that minimize carbon footprints and resource consumption.

How Are End-Use Applications Influencing the Demand for Pharmaceutical Equipment?

The demand for pharmaceutical manufacturing equipment is closely linked to the diverse applications across drug production segments, including oral solid dosage (OSD), parenteral drugs, biopharmaceuticals, and specialty medicines. The OSD segment, encompassing tablets and capsules, remains the largest consumer of manufacturing equipment, requiring advanced tablet presses, granulators, and coating machines to ensure precision and consistency. High-speed encapsulation machines are also in demand as manufacturers aim to enhance production efficiency while maintaining stringent quality control standards.

In the injectable and biopharmaceutical segments, the demand for aseptic processing equipment is surging due to the growing production of biologics, vaccines, and gene therapies. This includes advanced fill-finish systems, lyophilization (freeze-drying) technology, and isolators that maintain sterility throughout the manufacturing process. The rise in personalized medicine and small-batch biologics has further increased the need for flexible, modular manufacturing equipment that can handle variable production scales.

Additionally, the pharmaceutical packaging sector is witnessing significant technological advancements. Smart packaging solutions, such as anti-counterfeiting technology and track-and-trace systems, are becoming integral to pharmaceutical manufacturing. Serialization and aggregation equipment are critical components in ensuring compliance with global regulations like the Drug Supply Chain Security Act (DSCSA) and the Falsified Medicines Directive (FMD), which mandate stringent tracking of pharmaceutical products throughout the supply chain.

What Factors Are Driving the Growth of the Pharmaceutical Manufacturing Equipment Market?

The growth in the pharmaceutical manufacturing equipment market is driven by several factors, including the increasing demand for automation, rising production of biologics, and evolving regulatory requirements. The industry’s shift toward advanced manufacturing technologies, such as continuous processing, digital twin simulations, and robotics, is enhancing production efficiency and reducing operational costs. AI-powered predictive maintenance and real-time process analytics are further optimizing equipment utilization, minimizing downtime, and improving overall productivity.

The expansion of biopharmaceutical production is another major growth driver, with companies investing heavily in state-of-the-art bioprocessing equipment to meet the rising demand for monoclonal antibodies, mRNA-based therapies, and personalized medicine. Additionally, the pharmaceutical industry’s focus on sustainability and green manufacturing is driving investments in energy-efficient equipment and waste reduction technologies, aligning with global environmental standards.

Regulatory support for innovative manufacturing techniques, particularly continuous manufacturing and real-time quality control, is also accelerating market growth. Agencies like the FDA and EMA are encouraging pharmaceutical manufacturers to adopt advanced processing equipment that ensures drug quality and reduces production inefficiencies. Moreover, the expansion of CDMOs and contract manufacturing services is fueling demand for flexible and scalable production equipment that can handle diverse drug formulations and varying production volumes.

As the pharmaceutical industry continues to evolve, the demand for advanced manufacturing equipment will remain strong, shaping the future of drug production through automation, digitalization, and innovative processing technologies.

SCOPE OF STUDY:

The report analyzes the Pharmaceutical Impurity Synthesis and Isolation Services market in terms of units by the following Segments, and Geographic Regions/Countries:

Segments:

Service (Isolation Services, Analytical Services, Synthesis Services); Impurity (Inorganic Impurities, Organic Impurities, Residual Solvents); Technique (Chromatography Technique, Spectroscopy Technique, Crystallization Technique, Hyphenated Technique, Other Techniques); Application (Commercial Manufacturing Application, Drug Development Application, Quality Control Application, Regulatory Compliance Application); End-Use (Biotech & Pharmaceutical Companies End-Use, Contract Research Organizations End-Use, Other End-Uses)

Geographic Regions/Countries:

World; United States; Canada; Japan; China; Europe (France; Germany; Italy; United Kingdom; and Rest of Europe); Asia-Pacific; Rest of World.

Select Competitors (Total 43 Featured) -

  • Alfa Chemistry
  • Almac Group
  • BOC Sciences
  • Cambrex Corporation
  • Catalent, Inc.
  • Charles River Laboratories
  • Epichem
  • Eurofins Scientific
  • Frontage Laboratories
  • Intertek Group plc
  • Laboratory Corporation of America Holdings (Labcorp)
  • PCI Pharma Services
  • Pharmaron
  • Piramal Pharma Solutions
  • SGS Societe Generale de Surveillance SA
  • Symeres
  • Syngene International Limited
  • Veeda Clinical Research
  • Veeprho
  • WuXi AppTec

AI INTEGRATIONS

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TARIFF IMPACT FACTOR

Our new release incorporates impact of tariffs on geographical markets as we predict a shift in competitiveness of companies based on HQ country, manufacturing base, exports and imports (finished goods and OEM). This intricate and multifaceted market reality will impact competitors by increasing the Cost of Goods Sold (COGS), reducing profitability, reconfiguring supply chains, amongst other micro and macro market dynamics.

TABLE OF CONTENTS

I. METHODOLOGY

II. EXECUTIVE SUMMARY

  • 1. MARKET OVERVIEW
    • Influencer Market Insights
    • Tariff Impact on Global Supply Chain Patterns
    • Pharmaceutical Impurity Synthesis and Isolation Services - Global Key Competitors Percentage Market Share in 2025 (E)
    • Competitive Market Presence - Strong/Active/Niche/Trivial for Players Worldwide in 2025 (E)
  • 2. FOCUS ON SELECT PLAYERS
  • 3. MARKET TRENDS & DRIVERS
    • Rising Regulatory Pressure for Comprehensive Impurity Profiling Drives Demand for Specialized Synthesis and Isolation Services
    • Growth in Complex API Development Strengthens Business Case for Advanced Impurity Characterization Capabilities
    • Stringent ICH Guidelines on Impurity Limits and Identification Thresholds Propel Analytical and Isolation Service Adoption
    • Expanding Pipeline of Highly Potent and Targeted Therapeutics Throws the Spotlight on High-Fidelity Impurity Detection
    • Surge in Demand for Genotoxic and Nitrosamine Impurity Analysis Spurs Growth in Specialized Isolation Techniques
    • Outsourcing of Analytical R&D and Regulatory Submissions to CROs Accelerates Demand for Impurity Synthesis Partnerships
    • Increasing Use of High-Resolution Analytical Techniques (e.g., LC-MS/MS, NMR) Enhances Identification of Low-Level Impurities
    • Custom Synthesis of Reference Standards for Regulatory Submissions Expands Service Portfolio Scope
    • Rising Complexity of Synthetic Routes in Small Molecule APIs Generates Opportunities for Advanced Degradation Pathway Studies
    • Biopharmaceutical Growth and Rise of Complex Biologics Create Demand for Host Cell Protein and Process-Related Impurity Analysis
    • Growing Regulatory Emphasis on Data Integrity and Full Characterization Drives Process Development in Impurity Isolation
    • Strategic Collaborations Between Pharma and Analytical Service Providers Accelerate Turnaround Times and Compliance
    • Demand for Lifecycle Management of Drug Products Fuels Long-Term Impurity Monitoring and Requalification Services
    • Increasing Need for Customized, Scalable Isolation Techniques Supports Niche CRO and CDMO Engagements
  • 4. GLOBAL MARKET PERSPECTIVE
    • TABLE 1: World Pharmaceutical Impurity Synthesis and Isolation Services Market Analysis of Annual Sales in US$ Thousand for Years 2015 through 2030
    • TABLE 2: World Recent Past, Current & Future Analysis for Pharmaceutical Impurity Synthesis and Isolation Services by Geographic Region - USA, Canada, Japan, China, Europe, Asia-Pacific and Rest of World Markets - Independent Analysis of Annual Sales in US$ Thousand for Years 2024 through 2030 and % CAGR
    • TABLE 3: World 6-Year Perspective for Pharmaceutical Impurity Synthesis and Isolation Services by Geographic Region - Percentage Breakdown of Value Sales for USA, Canada, Japan, China, Europe, Asia-Pacific and Rest of World Markets for Years 2025 & 2030
    • TABLE 4: World Recent Past, Current & Future Analysis for Isolation Services by Geographic Region - USA, Canada, Japan, China, Europe, Asia-Pacific and Rest of World Markets - Independent Analysis of Annual Sales in US$ Thousand for Years 2024 through 2030 and % CAGR
    • TABLE 5: World 6-Year Perspective for Isolation Services by Geographic Region - Percentage Breakdown of Value Sales for USA, Canada, Japan, China, Europe, Asia-Pacific and Rest of World for Years 2025 & 2030
    • TABLE 6: World Recent Past, Current & Future Analysis for Analytical Services by Geographic Region - USA, Canada, Japan, China, Europe, Asia-Pacific and Rest of World Markets - Independent Analysis of Annual Sales in US$ Thousand for Years 2024 through 2030 and % CAGR
    • TABLE 7: World 6-Year Perspective for Analytical Services by Geographic Region - Percentage Breakdown of Value Sales for USA, Canada, Japan, China, Europe, Asia-Pacific and Rest of World for Years 2025 & 2030
    • TABLE 8: World Recent Past, Current & Future Analysis for Synthesis Services by Geographic Region - USA, Canada, Japan, China, Europe, Asia-Pacific and Rest of World Markets - Independent Analysis of Annual Sales in US$ Thousand for Years 2024 through 2030 and % CAGR
    • TABLE 9: World 6-Year Perspective for Synthesis Services by Geographic Region - Percentage Breakdown of Value Sales for USA, Canada, Japan, China, Europe, Asia-Pacific and Rest of World for Years 2025 & 2030
    • TABLE 10: World Recent Past, Current & Future Analysis for Hyphenated Technique by Geographic Region - USA, Canada, Japan, China, Europe, Asia-Pacific and Rest of World Markets - Independent Analysis of Annual Sales in US$ Thousand for Years 2024 through 2030 and % CAGR
    • TABLE 11: World 6-Year Perspective for Hyphenated Technique by Geographic Region - Percentage Breakdown of Value Sales for USA, Canada, Japan, China, Europe, Asia-Pacific and Rest of World for Years 2025 & 2030
    • TABLE 12: World Recent Past, Current & Future Analysis for Other Techniques by Geographic Region - USA, Canada, Japan, China, Europe, Asia-Pacific and Rest of World Markets - Independent Analysis of Annual Sales in US$ Thousand for Years 2024 through 2030 and % CAGR
    • TABLE 13: World 6-Year Perspective for Other Techniques by Geographic Region - Percentage Breakdown of Value Sales for USA, Canada, Japan, China, Europe, Asia-Pacific and Rest of World for Years 2025 & 2030
    • TABLE 14: World Recent Past, Current & Future Analysis for Chromatography Technique by Geographic Region - USA, Canada, Japan, China, Europe, Asia-Pacific and Rest of World Markets - Independent Analysis of Annual Sales in US$ Thousand for Years 2024 through 2030 and % CAGR
    • TABLE 15: World 6-Year Perspective for Chromatography Technique by Geographic Region - Percentage Breakdown of Value Sales for USA, Canada, Japan, China, Europe, Asia-Pacific and Rest of World for Years 2025 & 2030
    • TABLE 16: World Recent Past, Current & Future Analysis for Spectroscopy Technique by Geographic Region - USA, Canada, Japan, China, Europe, Asia-Pacific and Rest of World Markets - Independent Analysis of Annual Sales in US$ Thousand for Years 2024 through 2030 and % CAGR
    • TABLE 17: World 6-Year Perspective for Spectroscopy Technique by Geographic Region - Percentage Breakdown of Value Sales for USA, Canada, Japan, China, Europe, Asia-Pacific and Rest of World for Years 2025 & 2030
    • TABLE 18: World Recent Past, Current & Future Analysis for Crystallization Technique by Geographic Region - USA, Canada, Japan, China, Europe, Asia-Pacific and Rest of World Markets - Independent Analysis of Annual Sales in US$ Thousand for Years 2024 through 2030 and % CAGR
    • TABLE 19: World 6-Year Perspective for Crystallization Technique by Geographic Region - Percentage Breakdown of Value Sales for USA, Canada, Japan, China, Europe, Asia-Pacific and Rest of World for Years 2025 & 2030
    • TABLE 20: World Recent Past, Current & Future Analysis for Commercial Manufacturing Application by Geographic Region - USA, Canada, Japan, China, Europe, Asia-Pacific and Rest of World Markets - Independent Analysis of Annual Sales in US$ Thousand for Years 2024 through 2030 and % CAGR
    • TABLE 21: World 6-Year Perspective for Commercial Manufacturing Application by Geographic Region - Percentage Breakdown of Value Sales for USA, Canada, Japan, China, Europe, Asia-Pacific and Rest of World for Years 2025 & 2030
    • TABLE 22: World Recent Past, Current & Future Analysis for Drug Development Application by Geographic Region - USA, Canada, Japan, China, Europe, Asia-Pacific and Rest of World Markets - Independent Analysis of Annual Sales in US$ Thousand for Years 2024 through 2030 and % CAGR
    • TABLE 23: World 6-Year Perspective for Drug Development Application by Geographic Region - Percentage Breakdown of Value Sales for USA, Canada, Japan, China, Europe, Asia-Pacific and Rest of World for Years 2025 & 2030
    • TABLE 24: World Recent Past, Current & Future Analysis for Quality Control Application by Geographic Region - USA, Canada, Japan, China, Europe, Asia-Pacific and Rest of World Markets - Independent Analysis of Annual Sales in US$ Thousand for Years 2024 through 2030 and % CAGR
    • TABLE 25: World 6-Year Perspective for Quality Control Application by Geographic Region - Percentage Breakdown of Value Sales for USA, Canada, Japan, China, Europe, Asia-Pacific and Rest of World for Years 2025 & 2030
    • TABLE 26: World Recent Past, Current & Future Analysis for Regulatory Compliance Application by Geographic Region - USA, Canada, Japan, China, Europe, Asia-Pacific and Rest of World Markets - Independent Analysis of Annual Sales in US$ Thousand for Years 2024 through 2030 and % CAGR
    • TABLE 27: World 6-Year Perspective for Regulatory Compliance Application by Geographic Region - Percentage Breakdown of Value Sales for USA, Canada, Japan, China, Europe, Asia-Pacific and Rest of World for Years 2025 & 2030
    • TABLE 28: World Recent Past, Current & Future Analysis for Biotech & Pharmaceutical Companies End-Use by Geographic Region - USA, Canada, Japan, China, Europe, Asia-Pacific and Rest of World Markets - Independent Analysis of Annual Sales in US$ Thousand for Years 2024 through 2030 and % CAGR
    • TABLE 29: World 6-Year Perspective for Biotech & Pharmaceutical Companies End-Use by Geographic Region - Percentage Breakdown of Value Sales for USA, Canada, Japan, China, Europe, Asia-Pacific and Rest of World for Years 2025 & 2030
    • TABLE 30: World Recent Past, Current & Future Analysis for Contract Research Organizations End-Use by Geographic Region - USA, Canada, Japan, China, Europe, Asia-Pacific and Rest of World Markets - Independent Analysis of Annual Sales in US$ Thousand for Years 2024 through 2030 and % CAGR
    • TABLE 31: World 6-Year Perspective for Contract Research Organizations End-Use by Geographic Region - Percentage Breakdown of Value Sales for USA, Canada, Japan, China, Europe, Asia-Pacific and Rest of World for Years 2025 & 2030
    • TABLE 32: World Recent Past, Current & Future Analysis for Other End-Uses by Geographic Region - USA, Canada, Japan, China, Europe, Asia-Pacific and Rest of World Markets - Independent Analysis of Annual Sales in US$ Thousand for Years 2024 through 2030 and % CAGR
    • TABLE 33: World 6-Year Perspective for Other End-Uses by Geographic Region - Percentage Breakdown of Value Sales for USA, Canada, Japan, China, Europe, Asia-Pacific and Rest of World for Years 2025 & 2030
    • TABLE 34: World Recent Past, Current & Future Analysis for Inorganic Impurities by Geographic Region - USA, Canada, Japan, China, Europe, Asia-Pacific and Rest of World Markets - Independent Analysis of Annual Sales in US$ Thousand for Years 2024 through 2030 and % CAGR
    • TABLE 35: World 6-Year Perspective for Inorganic Impurities by Geographic Region - Percentage Breakdown of Value Sales for USA, Canada, Japan, China, Europe, Asia-Pacific and Rest of World for Years 2025 & 2030
    • TABLE 36: World Recent Past, Current & Future Analysis for Organic Impurities by Geographic Region - USA, Canada, Japan, China, Europe, Asia-Pacific and Rest of World Markets - Independent Analysis of Annual Sales in US$ Thousand for Years 2024 through 2030 and % CAGR
    • TABLE 37: World 6-Year Perspective for Organic Impurities by Geographic Region - Percentage Breakdown of Value Sales for USA, Canada, Japan, China, Europe, Asia-Pacific and Rest of World for Years 2025 & 2030
    • TABLE 38: World Recent Past, Current & Future Analysis for Residual Solvents by Geographic Region - USA, Canada, Japan, China, Europe, Asia-Pacific and Rest of World Markets - Independent Analysis of Annual Sales in US$ Thousand for Years 2024 through 2030 and % CAGR
    • TABLE 39: World 6-Year Perspective for Residual Solvents by Geographic Region - Percentage Breakdown of Value Sales for USA, Canada, Japan, China, Europe, Asia-Pacific and Rest of World for Years 2025 & 2030

III. MARKET ANALYSIS

  • UNITED STATES
    • Pharmaceutical Impurity Synthesis and Isolation Services Market Presence - Strong/Active/Niche/Trivial - Key Competitors in the United States for 2025 (E)
    • TABLE 40: USA Recent Past, Current & Future Analysis for Pharmaceutical Impurity Synthesis and Isolation Services by Service - Isolation Services, Analytical Services and Synthesis Services - Independent Analysis of Annual Sales in US$ Thousand for the Years 2024 through 2030 and % CAGR
    • TABLE 41: USA 6-Year Perspective for Pharmaceutical Impurity Synthesis and Isolation Services by Service - Percentage Breakdown of Value Sales for Isolation Services, Analytical Services and Synthesis Services for the Years 2025 & 2030
    • TABLE 42: USA Recent Past, Current & Future Analysis for Pharmaceutical Impurity Synthesis and Isolation Services by Technique - Hyphenated Technique, Other Techniques, Chromatography Technique, Spectroscopy Technique and Crystallization Technique - Independent Analysis of Annual Sales in US$ Thousand for the Years 2024 through 2030 and % CAGR
    • TABLE 43: USA 6-Year Perspective for Pharmaceutical Impurity Synthesis and Isolation Services by Technique - Percentage Breakdown of Value Sales for Hyphenated Technique, Other Techniques, Chromatography Technique, Spectroscopy Technique and Crystallization Technique for the Years 2025 & 2030
    • TABLE 44: USA Recent Past, Current & Future Analysis for Pharmaceutical Impurity Synthesis and Isolation Services by Application - Commercial Manufacturing Application, Drug Development Application, Quality Control Application and Regulatory Compliance Application - Independent Analysis of Annual Sales in US$ Thousand for the Years 2024 through 2030 and % CAGR
    • TABLE 45: USA 6-Year Perspective for Pharmaceutical Impurity Synthesis and Isolation Services by Application - Percentage Breakdown of Value Sales for Commercial Manufacturing Application, Drug Development Application, Quality Control Application and Regulatory Compliance Application for the Years 2025 & 2030
    • TABLE 46: USA Recent Past, Current & Future Analysis for Pharmaceutical Impurity Synthesis and Isolation Services by End-Use - Biotech & Pharmaceutical Companies End-Use, Contract Research Organizations End-Use and Other End-Uses - Independent Analysis of Annual Sales in US$ Thousand for the Years 2024 through 2030 and % CAGR
    • TABLE 47: USA 6-Year Perspective for Pharmaceutical Impurity Synthesis and Isolation Services by End-Use - Percentage Breakdown of Value Sales for Biotech & Pharmaceutical Companies End-Use, Contract Research Organizations End-Use and Other End-Uses for the Years 2025 & 2030
    • TABLE 48: USA Recent Past, Current & Future Analysis for Pharmaceutical Impurity Synthesis and Isolation Services by Impurity - Inorganic Impurities, Organic Impurities and Residual Solvents - Independent Analysis of Annual Sales in US$ Thousand for the Years 2024 through 2030 and % CAGR
    • TABLE 49: USA 6-Year Perspective for Pharmaceutical Impurity Synthesis and Isolation Services by Impurity - Percentage Breakdown of Value Sales for Inorganic Impurities, Organic Impurities and Residual Solvents for the Years 2025 & 2030
  • CANADA
    • TABLE 50: Canada Recent Past, Current & Future Analysis for Pharmaceutical Impurity Synthesis and Isolation Services by Service - Isolation Services, Analytical Services and Synthesis Services - Independent Analysis of Annual Sales in US$ Thousand for the Years 2024 through 2030 and % CAGR
    • TABLE 51: Canada 6-Year Perspective for Pharmaceutical Impurity Synthesis and Isolation Services by Service - Percentage Breakdown of Value Sales for Isolation Services, Analytical Services and Synthesis Services for the Years 2025 & 2030
    • TABLE 52: Canada Recent Past, Current & Future Analysis for Pharmaceutical Impurity Synthesis and Isolation Services by Technique - Hyphenated Technique, Other Techniques, Chromatography Technique, Spectroscopy Technique and Crystallization Technique - Independent Analysis of Annual Sales in US$ Thousand for the Years 2024 through 2030 and % CAGR
    • TABLE 53: Canada 6-Year Perspective for Pharmaceutical Impurity Synthesis and Isolation Services by Technique - Percentage Breakdown of Value Sales for Hyphenated Technique, Other Techniques, Chromatography Technique, Spectroscopy Technique and Crystallization Technique for the Years 2025 & 2030
    • TABLE 54: Canada Recent Past, Current & Future Analysis for Pharmaceutical Impurity Synthesis and Isolation Services by Application - Commercial Manufacturing Application, Drug Development Application, Quality Control Application and Regulatory Compliance Application - Independent Analysis of Annual Sales in US$ Thousand for the Years 2024 through 2030 and % CAGR
    • TABLE 55: Canada 6-Year Perspective for Pharmaceutical Impurity Synthesis and Isolation Services by Application - Percentage Breakdown of Value Sales for Commercial Manufacturing Application, Drug Development Application, Quality Control Application and Regulatory Compliance Application for the Years 2025 & 2030
    • TABLE 56: Canada Recent Past, Current & Future Analysis for Pharmaceutical Impurity Synthesis and Isolation Services by End-Use - Biotech & Pharmaceutical Companies End-Use, Contract Research Organizations End-Use and Other End-Uses - Independent Analysis of Annual Sales in US$ Thousand for the Years 2024 through 2030 and % CAGR
    • TABLE 57: Canada 6-Year Perspective for Pharmaceutical Impurity Synthesis and Isolation Services by End-Use - Percentage Breakdown of Value Sales for Biotech & Pharmaceutical Companies End-Use, Contract Research Organizations End-Use and Other End-Uses for the Years 2025 & 2030
    • TABLE 58: Canada Recent Past, Current & Future Analysis for Pharmaceutical Impurity Synthesis and Isolation Services by Impurity - Inorganic Impurities, Organic Impurities and Residual Solvents - Independent Analysis of Annual Sales in US$ Thousand for the Years 2024 through 2030 and % CAGR
    • TABLE 59: Canada 6-Year Perspective for Pharmaceutical Impurity Synthesis and Isolation Services by Impurity - Percentage Breakdown of Value Sales for Inorganic Impurities, Organic Impurities and Residual Solvents for the Years 2025 & 2030
  • JAPAN
    • Pharmaceutical Impurity Synthesis and Isolation Services Market Presence - Strong/Active/Niche/Trivial - Key Competitors in Japan for 2025 (E)
    • TABLE 60: Japan Recent Past, Current & Future Analysis for Pharmaceutical Impurity Synthesis and Isolation Services by Service - Isolation Services, Analytical Services and Synthesis Services - Independent Analysis of Annual Sales in US$ Thousand for the Years 2024 through 2030 and % CAGR
    • TABLE 61: Japan 6-Year Perspective for Pharmaceutical Impurity Synthesis and Isolation Services by Service - Percentage Breakdown of Value Sales for Isolation Services, Analytical Services and Synthesis Services for the Years 2025 & 2030
    • TABLE 62: Japan Recent Past, Current & Future Analysis for Pharmaceutical Impurity Synthesis and Isolation Services by Technique - Hyphenated Technique, Other Techniques, Chromatography Technique, Spectroscopy Technique and Crystallization Technique - Independent Analysis of Annual Sales in US$ Thousand for the Years 2024 through 2030 and % CAGR
    • TABLE 63: Japan 6-Year Perspective for Pharmaceutical Impurity Synthesis and Isolation Services by Technique - Percentage Breakdown of Value Sales for Hyphenated Technique, Other Techniques, Chromatography Technique, Spectroscopy Technique and Crystallization Technique for the Years 2025 & 2030
    • TABLE 64: Japan Recent Past, Current & Future Analysis for Pharmaceutical Impurity Synthesis and Isolation Services by Application - Commercial Manufacturing Application, Drug Development Application, Quality Control Application and Regulatory Compliance Application - Independent Analysis of Annual Sales in US$ Thousand for the Years 2024 through 2030 and % CAGR
    • TABLE 65: Japan 6-Year Perspective for Pharmaceutical Impurity Synthesis and Isolation Services by Application - Percentage Breakdown of Value Sales for Commercial Manufacturing Application, Drug Development Application, Quality Control Application and Regulatory Compliance Application for the Years 2025 & 2030
    • TABLE 66: Japan Recent Past, Current & Future Analysis for Pharmaceutical Impurity Synthesis and Isolation Services by End-Use - Biotech & Pharmaceutical Companies End-Use, Contract Research Organizations End-Use and Other End-Uses - Independent Analysis of Annual Sales in US$ Thousand for the Years 2024 through 2030 and % CAGR
    • TABLE 67: Japan 6-Year Perspective for Pharmaceutical Impurity Synthesis and Isolation Services by End-Use - Percentage Breakdown of Value Sales for Biotech & Pharmaceutical Companies End-Use, Contract Research Organizations End-Use and Other End-Uses for the Years 2025 & 2030
    • TABLE 68: Japan Recent Past, Current & Future Analysis for Pharmaceutical Impurity Synthesis and Isolation Services by Impurity - Inorganic Impurities, Organic Impurities and Residual Solvents - Independent Analysis of Annual Sales in US$ Thousand for the Years 2024 through 2030 and % CAGR
    • TABLE 69: Japan 6-Year Perspective for Pharmaceutical Impurity Synthesis and Isolation Services by Impurity - Percentage Breakdown of Value Sales for Inorganic Impurities, Organic Impurities and Residual Solvents for the Years 2025 & 2030
  • CHINA
    • Pharmaceutical Impurity Synthesis and Isolation Services Market Presence - Strong/Active/Niche/Trivial - Key Competitors in China for 2025 (E)
    • TABLE 70: China Recent Past, Current & Future Analysis for Pharmaceutical Impurity Synthesis and Isolation Services by Service - Isolation Services, Analytical Services and Synthesis Services - Independent Analysis of Annual Sales in US$ Thousand for the Years 2024 through 2030 and % CAGR
    • TABLE 71: China 6-Year Perspective for Pharmaceutical Impurity Synthesis and Isolation Services by Service - Percentage Breakdown of Value Sales for Isolation Services, Analytical Services and Synthesis Services for the Years 2025 & 2030
    • TABLE 72: China Recent Past, Current & Future Analysis for Pharmaceutical Impurity Synthesis and Isolation Services by Technique - Hyphenated Technique, Other Techniques, Chromatography Technique, Spectroscopy Technique and Crystallization Technique - Independent Analysis of Annual Sales in US$ Thousand for the Years 2024 through 2030 and % CAGR
    • TABLE 73: China 6-Year Perspective for Pharmaceutical Impurity Synthesis and Isolation Services by Technique - Percentage Breakdown of Value Sales for Hyphenated Technique, Other Techniques, Chromatography Technique, Spectroscopy Technique and Crystallization Technique for the Years 2025 & 2030
    • TABLE 74: China Recent Past, Current & Future Analysis for Pharmaceutical Impurity Synthesis and Isolation Services by Application - Commercial Manufacturing Application, Drug Development Application, Quality Control Application and Regulatory Compliance Application - Independent Analysis of Annual Sales in US$ Thousand for the Years 2024 through 2030 and % CAGR
    • TABLE 75: China 6-Year Perspective for Pharmaceutical Impurity Synthesis and Isolation Services by Application - Percentage Breakdown of Value Sales for Commercial Manufacturing Application, Drug Development Application, Quality Control Application and Regulatory Compliance Application for the Years 2025 & 2030
    • TABLE 76: China Recent Past, Current & Future Analysis for Pharmaceutical Impurity Synthesis and Isolation Services by End-Use - Biotech & Pharmaceutical Companies End-Use, Contract Research Organizations End-Use and Other End-Uses - Independent Analysis of Annual Sales in US$ Thousand for the Years 2024 through 2030 and % CAGR
    • TABLE 77: China 6-Year Perspective for Pharmaceutical Impurity Synthesis and Isolation Services by End-Use - Percentage Breakdown of Value Sales for Biotech & Pharmaceutical Companies End-Use, Contract Research Organizations End-Use and Other End-Uses for the Years 2025 & 2030
    • TABLE 78: China Recent Past, Current & Future Analysis for Pharmaceutical Impurity Synthesis and Isolation Services by Impurity - Inorganic Impurities, Organic Impurities and Residual Solvents - Independent Analysis of Annual Sales in US$ Thousand for the Years 2024 through 2030 and % CAGR
    • TABLE 79: China 6-Year Perspective for Pharmaceutical Impurity Synthesis and Isolation Services by Impurity - Percentage Breakdown of Value Sales for Inorganic Impurities, Organic Impurities and Residual Solvents for the Years 2025 & 2030
  • EUROPE
    • Pharmaceutical Impurity Synthesis and Isolation Services Market Presence - Strong/Active/Niche/Trivial - Key Competitors in Europe for 2025 (E)
    • TABLE 80: Europe Recent Past, Current & Future Analysis for Pharmaceutical Impurity Synthesis and Isolation Services by Geographic Region - France, Germany, Italy, UK and Rest of Europe Markets - Independent Analysis of Annual Sales in US$ Thousand for Years 2024 through 2030 and % CAGR
    • TABLE 81: Europe 6-Year Perspective for Pharmaceutical Impurity Synthesis and Isolation Services by Geographic Region - Percentage Breakdown of Value Sales for France, Germany, Italy, UK and Rest of Europe Markets for Years 2025 & 2030
    • TABLE 82: Europe Recent Past, Current & Future Analysis for Pharmaceutical Impurity Synthesis and Isolation Services by Service - Isolation Services, Analytical Services and Synthesis Services - Independent Analysis of Annual Sales in US$ Thousand for the Years 2024 through 2030 and % CAGR
    • TABLE 83: Europe 6-Year Perspective for Pharmaceutical Impurity Synthesis and Isolation Services by Service - Percentage Breakdown of Value Sales for Isolation Services, Analytical Services and Synthesis Services for the Years 2025 & 2030
    • TABLE 84: Europe Recent Past, Current & Future Analysis for Pharmaceutical Impurity Synthesis and Isolation Services by Technique - Hyphenated Technique, Other Techniques, Chromatography Technique, Spectroscopy Technique and Crystallization Technique - Independent Analysis of Annual Sales in US$ Thousand for the Years 2024 through 2030 and % CAGR
    • TABLE 85: Europe 6-Year Perspective for Pharmaceutical Impurity Synthesis and Isolation Services by Technique - Percentage Breakdown of Value Sales for Hyphenated Technique, Other Techniques, Chromatography Technique, Spectroscopy Technique and Crystallization Technique for the Years 2025 & 2030
    • TABLE 86: Europe Recent Past, Current & Future Analysis for Pharmaceutical Impurity Synthesis and Isolation Services by Application - Commercial Manufacturing Application, Drug Development Application, Quality Control Application and Regulatory Compliance Application - Independent Analysis of Annual Sales in US$ Thousand for the Years 2024 through 2030 and % CAGR
    • TABLE 87: Europe 6-Year Perspective for Pharmaceutical Impurity Synthesis and Isolation Services by Application - Percentage Breakdown of Value Sales for Commercial Manufacturing Application, Drug Development Application, Quality Control Application and Regulatory Compliance Application for the Years 2025 & 2030
    • TABLE 88: Europe Recent Past, Current & Future Analysis for Pharmaceutical Impurity Synthesis and Isolation Services by End-Use - Biotech & Pharmaceutical Companies End-Use, Contract Research Organizations End-Use and Other End-Uses - Independent Analysis of Annual Sales in US$ Thousand for the Years 2024 through 2030 and % CAGR
    • TABLE 89: Europe 6-Year Perspective for Pharmaceutical Impurity Synthesis and Isolation Services by End-Use - Percentage Breakdown of Value Sales for Biotech & Pharmaceutical Companies End-Use, Contract Research Organizations End-Use and Other End-Uses for the Years 2025 & 2030
    • TABLE 90: Europe Recent Past, Current & Future Analysis for Pharmaceutical Impurity Synthesis and Isolation Services by Impurity - Inorganic Impurities, Organic Impurities and Residual Solvents - Independent Analysis of Annual Sales in US$ Thousand for the Years 2024 through 2030 and % CAGR
    • TABLE 91: Europe 6-Year Perspective for Pharmaceutical Impurity Synthesis and Isolation Services by Impurity - Percentage Breakdown of Value Sales for Inorganic Impurities, Organic Impurities and Residual Solvents for the Years 2025 & 2030
  • FRANCE
    • Pharmaceutical Impurity Synthesis and Isolation Services Market Presence - Strong/Active/Niche/Trivial - Key Competitors in France for 2025 (E)
    • TABLE 92: France Recent Past, Current & Future Analysis for Pharmaceutical Impurity Synthesis and Isolation Services by Service - Isolation Services, Analytical Services and Synthesis Services - Independent Analysis of Annual Sales in US$ Thousand for the Years 2024 through 2030 and % CAGR
    • TABLE 93: France 6-Year Perspective for Pharmaceutical Impurity Synthesis and Isolation Services by Service - Percentage Breakdown of Value Sales for Isolation Services, Analytical Services and Synthesis Services for the Years 2025 & 2030
    • TABLE 94: France Recent Past, Current & Future Analysis for Pharmaceutical Impurity Synthesis and Isolation Services by Technique - Hyphenated Technique, Other Techniques, Chromatography Technique, Spectroscopy Technique and Crystallization Technique - Independent Analysis of Annual Sales in US$ Thousand for the Years 2024 through 2030 and % CAGR
    • TABLE 95: France 6-Year Perspective for Pharmaceutical Impurity Synthesis and Isolation Services by Technique - Percentage Breakdown of Value Sales for Hyphenated Technique, Other Techniques, Chromatography Technique, Spectroscopy Technique and Crystallization Technique for the Years 2025 & 2030
    • TABLE 96: France Recent Past, Current & Future Analysis for Pharmaceutical Impurity Synthesis and Isolation Services by Application - Commercial Manufacturing Application, Drug Development Application, Quality Control Application and Regulatory Compliance Application - Independent Analysis of Annual Sales in US$ Thousand for the Years 2024 through 2030 and % CAGR
    • TABLE 97: France 6-Year Perspective for Pharmaceutical Impurity Synthesis and Isolation Services by Application - Percentage Breakdown of Value Sales for Commercial Manufacturing Application, Drug Development Application, Quality Control Application and Regulatory Compliance Application for the Years 2025 & 2030
    • TABLE 98: France Recent Past, Current & Future Analysis for Pharmaceutical Impurity Synthesis and Isolation Services by End-Use - Biotech & Pharmaceutical Companies End-Use, Contract Research Organizations End-Use and Other End-Uses - Independent Analysis of Annual Sales in US$ Thousand for the Years 2024 through 2030 and % CAGR
    • TABLE 99: France 6-Year Perspective for Pharmaceutical Impurity Synthesis and Isolation Services by End-Use - Percentage Breakdown of Value Sales for Biotech & Pharmaceutical Companies End-Use, Contract Research Organizations End-Use and Other End-Uses for the Years 2025 & 2030
    • TABLE 100: France Recent Past, Current & Future Analysis for Pharmaceutical Impurity Synthesis and Isolation Services by Impurity - Inorganic Impurities, Organic Impurities and Residual Solvents - Independent Analysis of Annual Sales in US$ Thousand for the Years 2024 through 2030 and % CAGR
    • TABLE 101: France 6-Year Perspective for Pharmaceutical Impurity Synthesis and Isolation Services by Impurity - Percentage Breakdown of Value Sales for Inorganic Impurities, Organic Impurities and Residual Solvents for the Years 2025 & 2030
  • GERMANY
    • Pharmaceutical Impurity Synthesis and Isolation Services Market Presence - Strong/Active/Niche/Trivial - Key Competitors in Germany for 2025 (E)
    • TABLE 102: Germany Recent Past, Current & Future Analysis for Pharmaceutical Impurity Synthesis and Isolation Services by Service - Isolation Services, Analytical Services and Synthesis Services - Independent Analysis of Annual Sales in US$ Thousand for the Years 2024 through 2030 and % CAGR
    • TABLE 103: Germany 6-Year Perspective for Pharmaceutical Impurity Synthesis and Isolation Services by Service - Percentage Breakdown of Value Sales for Isolation Services, Analytical Services and Synthesis Services for the Years 2025 & 2030
    • TABLE 104: Germany Recent Past, Current & Future Analysis for Pharmaceutical Impurity Synthesis and Isolation Services by Technique - Hyphenated Technique, Other Techniques, Chromatography Technique, Spectroscopy Technique and Crystallization Technique - Independent Analysis of Annual Sales in US$ Thousand for the Years 2024 through 2030 and % CAGR
    • TABLE 105: Germany 6-Year Perspective for Pharmaceutical Impurity Synthesis and Isolation Services by Technique - Percentage Breakdown of Value Sales for Hyphenated Technique, Other Techniques, Chromatography Technique, Spectroscopy Technique and Crystallization Technique for the Years 2025 & 2030
    • TABLE 106: Germany Recent Past, Current & Future Analysis for Pharmaceutical Impurity Synthesis and Isolation Services by Application - Commercial Manufacturing Application, Drug Development Application, Quality Control Application and Regulatory Compliance Application - Independent Analysis of Annual Sales in US$ Thousand for the Years 2024 through 2030 and % CAGR
    • TABLE 107: Germany 6-Year Perspective for Pharmaceutical Impurity Synthesis and Isolation Services by Application - Percentage Breakdown of Value Sales for Commercial Manufacturing Application, Drug Development Application, Quality Control Application and Regulatory Compliance Application for the Years 2025 & 2030
    • TABLE 108: Germany Recent Past, Current & Future Analysis for Pharmaceutical Impurity Synthesis and Isolation Services by End-Use - Biotech & Pharmaceutical Companies End-Use, Contract Research Organizations End-Use and Other End-Uses - Independent Analysis of Annual Sales in US$ Thousand for the Years 2024 through 2030 and % CAGR
    • TABLE 109: Germany 6-Year Perspective for Pharmaceutical Impurity Synthesis and Isolation Services by End-Use - Percentage Breakdown of Value Sales for Biotech & Pharmaceutical Companies End-Use, Contract Research Organizations End-Use and Other End-Uses for the Years 2025 & 2030
    • TABLE 110: Germany Recent Past, Current & Future Analysis for Pharmaceutical Impurity Synthesis and Isolation Services by Impurity - Inorganic Impurities, Organic Impurities and Residual Solvents - Independent Analysis of Annual Sales in US$ Thousand for the Years 2024 through 2030 and % CAGR
    • TABLE 111: Germany 6-Year Perspective for Pharmaceutical Impurity Synthesis and Isolation Services by Impurity - Percentage Breakdown of Value Sales for Inorganic Impurities, Organic Impurities and Residual Solvents for the Years 2025 & 2030
  • ITALY
    • TABLE 112: Italy Recent Past, Current & Future Analysis for Pharmaceutical Impurity Synthesis and Isolation Services by Service - Isolation Services, Analytical Services and Synthesis Services - Independent Analysis of Annual Sales in US$ Thousand for the Years 2024 through 2030 and % CAGR
    • TABLE 113: Italy 6-Year Perspective for Pharmaceutical Impurity Synthesis and Isolation Services by Service - Percentage Breakdown of Value Sales for Isolation Services, Analytical Services and Synthesis Services for the Years 2025 & 2030
    • TABLE 114: Italy Recent Past, Current & Future Analysis for Pharmaceutical Impurity Synthesis and Isolation Services by Technique - Hyphenated Technique, Other Techniques, Chromatography Technique, Spectroscopy Technique and Crystallization Technique - Independent Analysis of Annual Sales in US$ Thousand for the Years 2024 through 2030 and % CAGR
    • TABLE 115: Italy 6-Year Perspective for Pharmaceutical Impurity Synthesis and Isolation Services by Technique - Percentage Breakdown of Value Sales for Hyphenated Technique, Other Techniques, Chromatography Technique, Spectroscopy Technique and Crystallization Technique for the Years 2025 & 2030
    • TABLE 116: Italy Recent Past, Current & Future Analysis for Pharmaceutical Impurity Synthesis and Isolation Services by Application - Commercial Manufacturing Application, Drug Development Application, Quality Control Application and Regulatory Compliance Application - Independent Analysis of Annual Sales in US$ Thousand for the Years 2024 through 2030 and % CAGR
    • TABLE 117: Italy 6-Year Perspective for Pharmaceutical Impurity Synthesis and Isolation Services by Application - Percentage Breakdown of Value Sales for Commercial Manufacturing Application, Drug Development Application, Quality Control Application and Regulatory Compliance Application for the Years 2025 & 2030
    • TABLE 118: Italy Recent Past, Current & Future Analysis for Pharmaceutical Impurity Synthesis and Isolation Services by End-Use - Biotech & Pharmaceutical Companies End-Use, Contract Research Organizations End-Use and Other End-Uses - Independent Analysis of Annual Sales in US$ Thousand for the Years 2024 through 2030 and % CAGR
    • TABLE 119: Italy 6-Year Perspective for Pharmaceutical Impurity Synthesis and Isolation Services by End-Use - Percentage Breakdown of Value Sales for Biotech & Pharmaceutical Companies End-Use, Contract Research Organizations End-Use and Other End-Uses for the Years 2025 & 2030
    • TABLE 120: Italy Recent Past, Current & Future Analysis for Pharmaceutical Impurity Synthesis and Isolation Services by Impurity - Inorganic Impurities, Organic Impurities and Residual Solvents - Independent Analysis of Annual Sales in US$ Thousand for the Years 2024 through 2030 and % CAGR
    • TABLE 121: Italy 6-Year Perspective for Pharmaceutical Impurity Synthesis and Isolation Services by Impurity - Percentage Breakdown of Value Sales for Inorganic Impurities, Organic Impurities and Residual Solvents for the Years 2025 & 2030
  • UNITED KINGDOM
    • Pharmaceutical Impurity Synthesis and Isolation Services Market Presence - Strong/Active/Niche/Trivial - Key Competitors in the United Kingdom for 2025 (E)
    • TABLE 122: UK Recent Past, Current & Future Analysis for Pharmaceutical Impurity Synthesis and Isolation Services by Service - Isolation Services, Analytical Services and Synthesis Services - Independent Analysis of Annual Sales in US$ Thousand for the Years 2024 through 2030 and % CAGR
    • TABLE 123: UK 6-Year Perspective for Pharmaceutical Impurity Synthesis and Isolation Services by Service - Percentage Breakdown of Value Sales for Isolation Services, Analytical Services and Synthesis Services for the Years 2025 & 2030
    • TABLE 124: UK Recent Past, Current & Future Analysis for Pharmaceutical Impurity Synthesis and Isolation Services by Technique - Hyphenated Technique, Other Techniques, Chromatography Technique, Spectroscopy Technique and Crystallization Technique - Independent Analysis of Annual Sales in US$ Thousand for the Years 2024 through 2030 and % CAGR
    • TABLE 125: UK 6-Year Perspective for Pharmaceutical Impurity Synthesis and Isolation Services by Technique - Percentage Breakdown of Value Sales for Hyphenated Technique, Other Techniques, Chromatography Technique, Spectroscopy Technique and Crystallization Technique for the Years 2025 & 2030
    • TABLE 126: UK Recent Past, Current & Future Analysis for Pharmaceutical Impurity Synthesis and Isolation Services by Application - Commercial Manufacturing Application, Drug Development Application, Quality Control Application and Regulatory Compliance Application - Independent Analysis of Annual Sales in US$ Thousand for the Years 2024 through 2030 and % CAGR
    • TABLE 127: UK 6-Year Perspective for Pharmaceutical Impurity Synthesis and Isolation Services by Application - Percentage Breakdown of Value Sales for Commercial Manufacturing Application, Drug Development Application, Quality Control Application and Regulatory Compliance Application for the Years 2025 & 2030
    • TABLE 128: UK Recent Past, Current & Future Analysis for Pharmaceutical Impurity Synthesis and Isolation Services by End-Use - Biotech & Pharmaceutical Companies End-Use, Contract Research Organizations End-Use and Other End-Uses - Independent Analysis of Annual Sales in US$ Thousand for the Years 2024 through 2030 and % CAGR
    • TABLE 129: UK 6-Year Perspective for Pharmaceutical Impurity Synthesis and Isolation Services by End-Use - Percentage Breakdown of Value Sales for Biotech & Pharmaceutical Companies End-Use, Contract Research Organizations End-Use and Other End-Uses for the Years 2025 & 2030
    • TABLE 130: UK Recent Past, Current & Future Analysis for Pharmaceutical Impurity Synthesis and Isolation Services by Impurity - Inorganic Impurities, Organic Impurities and Residual Solvents - Independent Analysis of Annual Sales in US$ Thousand for the Years 2024 through 2030 and % CAGR
    • TABLE 131: UK 6-Year Perspective for Pharmaceutical Impurity Synthesis and Isolation Services by Impurity - Percentage Breakdown of Value Sales for Inorganic Impurities, Organic Impurities and Residual Solvents for the Years 2025 & 2030
  • REST OF EUROPE
    • TABLE 132: Rest of Europe Recent Past, Current & Future Analysis for Pharmaceutical Impurity Synthesis and Isolation Services by Service - Isolation Services, Analytical Services and Synthesis Services - Independent Analysis of Annual Sales in US$ Thousand for the Years 2024 through 2030 and % CAGR
    • TABLE 133: Rest of Europe 6-Year Perspective for Pharmaceutical Impurity Synthesis and Isolation Services by Service - Percentage Breakdown of Value Sales for Isolation Services, Analytical Services and Synthesis Services for the Years 2025 & 2030
    • TABLE 134: Rest of Europe Recent Past, Current & Future Analysis for Pharmaceutical Impurity Synthesis and Isolation Services by Technique - Hyphenated Technique, Other Techniques, Chromatography Technique, Spectroscopy Technique and Crystallization Technique - Independent Analysis of Annual Sales in US$ Thousand for the Years 2024 through 2030 and % CAGR
    • TABLE 135: Rest of Europe 6-Year Perspective for Pharmaceutical Impurity Synthesis and Isolation Services by Technique - Percentage Breakdown of Value Sales for Hyphenated Technique, Other Techniques, Chromatography Technique, Spectroscopy Technique and Crystallization Technique for the Years 2025 & 2030
    • TABLE 136: Rest of Europe Recent Past, Current & Future Analysis for Pharmaceutical Impurity Synthesis and Isolation Services by Application - Commercial Manufacturing Application, Drug Development Application, Quality Control Application and Regulatory Compliance Application - Independent Analysis of Annual Sales in US$ Thousand for the Years 2024 through 2030 and % CAGR
    • TABLE 137: Rest of Europe 6-Year Perspective for Pharmaceutical Impurity Synthesis and Isolation Services by Application - Percentage Breakdown of Value Sales for Commercial Manufacturing Application, Drug Development Application, Quality Control Application and Regulatory Compliance Application for the Years 2025 & 2030
    • TABLE 138: Rest of Europe Recent Past, Current & Future Analysis for Pharmaceutical Impurity Synthesis and Isolation Services by End-Use - Biotech & Pharmaceutical Companies End-Use, Contract Research Organizations End-Use and Other End-Uses - Independent Analysis of Annual Sales in US$ Thousand for the Years 2024 through 2030 and % CAGR
    • TABLE 139: Rest of Europe 6-Year Perspective for Pharmaceutical Impurity Synthesis and Isolation Services by End-Use - Percentage Breakdown of Value Sales for Biotech & Pharmaceutical Companies End-Use, Contract Research Organizations End-Use and Other End-Uses for the Years 2025 & 2030
    • TABLE 140: Rest of Europe Recent Past, Current & Future Analysis for Pharmaceutical Impurity Synthesis and Isolation Services by Impurity - Inorganic Impurities, Organic Impurities and Residual Solvents - Independent Analysis of Annual Sales in US$ Thousand for the Years 2024 through 2030 and % CAGR
    • TABLE 141: Rest of Europe 6-Year Perspective for Pharmaceutical Impurity Synthesis and Isolation Services by Impurity - Percentage Breakdown of Value Sales for Inorganic Impurities, Organic Impurities and Residual Solvents for the Years 2025 & 2030
  • ASIA-PACIFIC
    • Pharmaceutical Impurity Synthesis and Isolation Services Market Presence - Strong/Active/Niche/Trivial - Key Competitors in Asia-Pacific for 2025 (E)
    • TABLE 142: Asia-Pacific Recent Past, Current & Future Analysis for Pharmaceutical Impurity Synthesis and Isolation Services by Service - Isolation Services, Analytical Services and Synthesis Services - Independent Analysis of Annual Sales in US$ Thousand for the Years 2024 through 2030 and % CAGR
    • TABLE 143: Asia-Pacific 6-Year Perspective for Pharmaceutical Impurity Synthesis and Isolation Services by Service - Percentage Breakdown of Value Sales for Isolation Services, Analytical Services and Synthesis Services for the Years 2025 & 2030
    • TABLE 144: Asia-Pacific Recent Past, Current & Future Analysis for Pharmaceutical Impurity Synthesis and Isolation Services by Technique - Hyphenated Technique, Other Techniques, Chromatography Technique, Spectroscopy Technique and Crystallization Technique - Independent Analysis of Annual Sales in US$ Thousand for the Years 2024 through 2030 and % CAGR
    • TABLE 145: Asia-Pacific 6-Year Perspective for Pharmaceutical Impurity Synthesis and Isolation Services by Technique - Percentage Breakdown of Value Sales for Hyphenated Technique, Other Techniques, Chromatography Technique, Spectroscopy Technique and Crystallization Technique for the Years 2025 & 2030
    • TABLE 146: Asia-Pacific Recent Past, Current & Future Analysis for Pharmaceutical Impurity Synthesis and Isolation Services by Application - Commercial Manufacturing Application, Drug Development Application, Quality Control Application and Regulatory Compliance Application - Independent Analysis of Annual Sales in US$ Thousand for the Years 2024 through 2030 and % CAGR
    • TABLE 147: Asia-Pacific 6-Year Perspective for Pharmaceutical Impurity Synthesis and Isolation Services by Application - Percentage Breakdown of Value Sales for Commercial Manufacturing Application, Drug Development Application, Quality Control Application and Regulatory Compliance Application for the Years 2025 & 2030
    • TABLE 148: Asia-Pacific Recent Past, Current & Future Analysis for Pharmaceutical Impurity Synthesis and Isolation Services by End-Use - Biotech & Pharmaceutical Companies End-Use, Contract Research Organizations End-Use and Other End-Uses - Independent Analysis of Annual Sales in US$ Thousand for the Years 2024 through 2030 and % CAGR
    • TABLE 149: Asia-Pacific 6-Year Perspective for Pharmaceutical Impurity Synthesis and Isolation Services by End-Use - Percentage Breakdown of Value Sales for Biotech & Pharmaceutical Companies End-Use, Contract Research Organizations End-Use and Other End-Uses for the Years 2025 & 2030
    • TABLE 150: Asia-Pacific Recent Past, Current & Future Analysis for Pharmaceutical Impurity Synthesis and Isolation Services by Impurity - Inorganic Impurities, Organic Impurities and Residual Solvents - Independent Analysis of Annual Sales in US$ Thousand for the Years 2024 through 2030 and % CAGR
    • TABLE 151: Asia-Pacific 6-Year Perspective for Pharmaceutical Impurity Synthesis and Isolation Services by Impurity - Percentage Breakdown of Value Sales for Inorganic Impurities, Organic Impurities and Residual Solvents for the Years 2025 & 2030
  • REST OF WORLD
    • TABLE 152: Rest of World Recent Past, Current & Future Analysis for Pharmaceutical Impurity Synthesis and Isolation Services by Service - Isolation Services, Analytical Services and Synthesis Services - Independent Analysis of Annual Sales in US$ Thousand for the Years 2024 through 2030 and % CAGR
    • TABLE 153: Rest of World 6-Year Perspective for Pharmaceutical Impurity Synthesis and Isolation Services by Service - Percentage Breakdown of Value Sales for Isolation Services, Analytical Services and Synthesis Services for the Years 2025 & 2030
    • TABLE 154: Rest of World Recent Past, Current & Future Analysis for Pharmaceutical Impurity Synthesis and Isolation Services by Technique - Hyphenated Technique, Other Techniques, Chromatography Technique, Spectroscopy Technique and Crystallization Technique - Independent Analysis of Annual Sales in US$ Thousand for the Years 2024 through 2030 and % CAGR
    • TABLE 155: Rest of World 6-Year Perspective for Pharmaceutical Impurity Synthesis and Isolation Services by Technique - Percentage Breakdown of Value Sales for Hyphenated Technique, Other Techniques, Chromatography Technique, Spectroscopy Technique and Crystallization Technique for the Years 2025 & 2030
    • TABLE 156: Rest of World Recent Past, Current & Future Analysis for Pharmaceutical Impurity Synthesis and Isolation Services by Application - Commercial Manufacturing Application, Drug Development Application, Quality Control Application and Regulatory Compliance Application - Independent Analysis of Annual Sales in US$ Thousand for the Years 2024 through 2030 and % CAGR
    • TABLE 157: Rest of World 6-Year Perspective for Pharmaceutical Impurity Synthesis and Isolation Services by Application - Percentage Breakdown of Value Sales for Commercial Manufacturing Application, Drug Development Application, Quality Control Application and Regulatory Compliance Application for the Years 2025 & 2030
    • TABLE 158: Rest of World Recent Past, Current & Future Analysis for Pharmaceutical Impurity Synthesis and Isolation Services by End-Use - Biotech & Pharmaceutical Companies End-Use, Contract Research Organizations End-Use and Other End-Uses - Independent Analysis of Annual Sales in US$ Thousand for the Years 2024 through 2030 and % CAGR
    • TABLE 159: Rest of World 6-Year Perspective for Pharmaceutical Impurity Synthesis and Isolation Services by End-Use - Percentage Breakdown of Value Sales for Biotech & Pharmaceutical Companies End-Use, Contract Research Organizations End-Use and Other End-Uses for the Years 2025 & 2030
    • TABLE 160: Rest of World Recent Past, Current & Future Analysis for Pharmaceutical Impurity Synthesis and Isolation Services by Impurity - Inorganic Impurities, Organic Impurities and Residual Solvents - Independent Analysis of Annual Sales in US$ Thousand for the Years 2024 through 2030 and % CAGR
    • TABLE 161: Rest of World 6-Year Perspective for Pharmaceutical Impurity Synthesis and Isolation Services by Impurity - Percentage Breakdown of Value Sales for Inorganic Impurities, Organic Impurities and Residual Solvents for the Years 2025 & 2030

IV. COMPETITION

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