시장보고서
상품코드
1839308

세계의 바이오프로세스 밸리데이션 시장 규모, 점유율, 업계 분석 리포트 : 모드별, 스테이지별, 시험 유형별, 지역별 전망 및 예측(2025-2032년)

Global Bioprocess Validation Market Size, Share & Industry Analysis Report By Mode, By Stage, By Testing Type, By Regional Outlook and Forecast, 2025 - 2032

발행일: | 리서치사: KBV Research | 페이지 정보: 영문 480 Pages | 배송안내 : 즉시배송

    
    
    



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

바이오프로세스 밸리데이션 시장 규모는 예측 기간 중 8.8%의 CAGR로 시장 성장하며, 2032년까지 9억 9,402만 달러에 달할 것으로 예상됩니다.

주요 하이라이트:

  • 북미 시장은 2024년 바이오프로세스 밸리데이션 시장을 장악하여 2024년 40.00%의 매출 점유율을 차지했습니다.
  • 미국 시장은 2032년까지 시장 규모가 2억 6,419만 달러에 달할 것으로 예상되며, 북미 시장에서의 리더십을 유지할 것으로 전망됩니다.
  • 다양한 모드 중 사내 부문이 2024년 매출 점유율의 79.67%를 차지하며 세계 시장을 장악했습니다.
  • 단계별로는 지속적인 프로세스 검증 부문이 2032년까지 39.15%의 매출 점유율을 차지하며 세계 시장을 주도할 것으로 예측됩니다.
  • 바이오프로세스 잔류물 테스트는 2024년 주요 테스트 유형으로 부상하여 28.13%의 매출 점유율을 획득하며, 예측 기간 중에도 우위성을 유지할 것으로 예측됩니다.

바이오프로세스 밸리데이션 시장은 개발 후 진행되는 적격성 평가 활동에서 규제 당국의 기대, 신기술 및 새로운 바이오의약품에 의해 형성되는 통합된 수명주기 중심의 분야로 변화하고 있습니다. 검증은 과거에는 정적 배치 수준의 점검에 중점을 두었지만, 현재는 위험 기반 접근 방식, 지속적인 모니터링 및 데이터베이스 모니터링에 중점을 두고 있습니다. 일회용 시스템, 연속 바이오프로세스, 실시간 분석과 같은 새로운 기술의 등장으로 요구사항이 변화하고 있으며, 일회용 제품, 추출물, 침출물, 그리고 모듈식 시스템의 검증이 필요하게 되었습니다. FDA와 EMA는 수명주기 및 리스크 기반 프레임워크를 추진하고 있으며, OEM과 서비스 프로바이더는 디지털 플랫폼, 시뮬레이션 툴 및 프로세스 분석 기술을 사용하여 보다 신속하고 능동적으로 검증을 수행하고 있습니다. 아시아태평양에서 바이오 제약 기업이 사업을 확장하고 아웃소싱이 보편화되고 있는 것도 시장 성장을 지원하고 있습니다. CDMO와 전문 서비스 프로바이더의 역할이 확대되고 있습니다.

주요 동향으로는 예측 모델링, 실시간 센서, 클라우드 기반 분석을 통한 디지털화 및 지속적인 검증, 일회용 기술의 완전한 검증, CDMO 및 전문 업체로의 아웃소싱 증가 등을 들 수 있습니다. 각국의 규제 요구에 대응하기 위해 주요 기업은 하드웨어 제품에 검증 기능 추가, 서비스 번들링, 신규 분야 진출 등의 전략을 채택하고 있습니다. 경쟁 구도는 Sartorius, Pall, Thermo Fisher와 같은 대형 OEM과 속도, 유연성, 틈새 전문성을 바탕으로 경쟁하는 민첩한 전문 검증 프로바이더들 사이에서 균형을 이루고 있습니다. 검증이 더욱 디지털화, 리스크 기반, 그리고 지속적으로 이루어짐에 따라 규제적 신뢰성과 새로운 아이디어, 그리고 확장 가능한 서비스 모델을 결합하는 기업이 성장하고 세분화되는 시장에서 경쟁력을 유지할 수 있을 것입니다.

시장 점유율 분석

COVID-19의 영향 분석

COVID-19 팬데믹은 전 세계 공급망의 혼란, 운송 지연, 원자재 및 장비 수급의 어려움으로 인해 바이오프로세스 밸리데이션 시장에 큰 타격을 입혔습니다. 봉쇄와 사회적 거리두기로 인해 사람들의 취업이 어려워지고, 검증 활동이 정체되고, 제품 개발이 지연되었습니다. COVID-19 치료제와 백신에 집중하면서 제약업계의 다른 분야에 대한 검증의 필요성이 줄어들었습니다. 또한 경제의 불확실성으로 인해 기업은 R&D 및 컴플라이언스 예산을 줄이고, 검증 프로젝트가 지연되고, 시장 출시 기간이 길어졌습니다. 전반적으로 이러한 것은 팬데믹 기간 중 업무상의 문제, 매출 감소, 시장 성장률 하락을 초래했습니다. 이처럼 COVID-19 팬데믹은 시장에 부정적인 영향을 미쳤습니다.

무대 전망

단계에 따라 지속적 공정 검증, 공정 적격성 평가, 공정 설계로 구분됩니다. 공정 적격성 평가 부문은 2024년 바이오프로세스 밸리데이션 시장에서 31%의 매출 점유율을 기록할 것으로 예측됩니다. 이 단계에서는 바이오프로세스 장비, 시스템 및 유틸리티가 사전에 정의된 수용 기준 내에서 일관되게 작동한다는 것을 입증하는 데 중점을 둡니다. 이는 공정 설계와 대규모 생산 사이의 간극을 메우고 설정된 매개 변수가 작동 조건에서 유지되도록 보장하는 중요한 단계입니다.

시험 유형 전망

테스트 유형에 따라 시장은 바이오프로세스 잔류물 테스트, 추출물 및 침출물 테스트, 바이러스 클리어런스 테스트, 무선 및 IoT 침투 테스트 및 기타 테스트 유형으로 분류됩니다. 추출물 및 침출물 테스트 부문은 2024년 바이오프로세스 밸리데이션 시장에서 25%의 매출 점유율을 차지했습니다.현대 바이오 제조에서 일회용 시스템, 일회용 바이오리액터, 폴리머 기반 튜브 및 포장재에 대한 의존도가 높아짐에 따라 잠재적으로 유해한 물질이 최종 제품으로 유출될 수 있다는 우려가 커지고 있습니다.

지역 전망

지역별로 바이오프로세스 밸리데이션 시장은 북미, 유럽, 아시아태평양, LAMEA, 기타 지역으로 분석됩니다. 북미 부문은 2024년 바이오프로세스 밸리데이션 시장에서 40%의 매출 점유율을 기록할 것으로 예측됩니다. 북미와 유럽은 바이오의약품 산업이 확립되어 있고, 규제 체계가 엄격하며, 제조 인프라가 첨단화되어 있으며, 바이오프로세스 밸리데이션 시장에서 가장 큰 점유율을 차지하고 있습니다. 미국은 FDA의 강력한 감독, 많은 바이오제약 기업, 그리고 단클론 항체, 백신, 세포 및 유전자 치료와 같은 새로운 치료법에 많은 자금이 투입되고 있으며, 북미의 선두주자입니다. 유럽은 EMA의 수명주기 기반 검증 가이드라인에 힘입어 규제 주도형 혁신의 중심지가 되고 있습니다. 독일, 스위스, 영국 등 국가에는 주요 바이오의약품 클러스터가 있습니다. 두 지역 모두 컴플라이언스, 리스크 기반 검증, 지속적인 모니터링에 중점을 두고 있습니다. 따라서 첨단 검증 서비스와 연동되는 디지털 툴이 절실히 요구되고 있습니다.

아시아태평양 및 LAMEA(멕시코 제외)는 바이오의약품 제조의 성장과 품질에 대한 규제 강화로 인해 고성장 지역으로 부상하고 있습니다. 중국, 인도, 한국, 일본 등 아시아태평양 국가들은 바이오의약품 생산 능력에 많은 자금을 투자하고 있습니다. 이에 따라 일회용 시스템, 연속 처리, 아웃소싱된 CDMO 서비스 검증의 필요성이 높아지고 있습니다. 한편, LAMEA에서는 브라질, 사우디아라비아, UAE, 남아프리카공화국이 헬스케어 제조 다각화를 위한 정부 프로그램의 지원을 받아 바이오의약품 부문을 점차 강화하고 있습니다. 이들 지역에서는 세계 표준을 충족하기 위해 외부 검증 프로바이더에 대한 의존도가 높아지고 있으며, 이는 다국적 OEM과 지역 전문 기업 모두에게 사업 확장의 기회를 제공합니다.

목차

제1장 시장 범위와 조사 방법

  • 시장의 정의
  • 목적
  • 시장 범위
  • 세분화
  • 조사 방법

제2장 시장 개관

  • 주요 하이라이트

제3장 시장 개요

  • 서론
    • 개요
      • 시장 구성과 시나리오
  • 시장에 영향을 미치는 주요 요인
    • 시장 성장 촉진요인
    • 시장 성장 억제요인
    • 시장 기회
    • 시장이 해결해야 할 과제

제4장 시장 동향 - 바이오프로세스 밸리데이션 시장

제5장 경쟁의 현황 - 바이오프로세스 밸리데이션 시장

제6장 바이오프로세스 밸리데이션 시장의 밸류체인 분석

제7장 제품수명주기 - 바이오프로세스 밸리데이션 시장

제8장 시장 통합 - 바이오프로세스 밸리데이션 시장

제9장 주요 고객 기준 - 바이오프로세스 밸리데이션 시장

제10장 경쟁 분석 - 세계

  • 시장 점유율 분석 2024
  • 바이오프로세스 밸리데이션 시장에서 최근 전략
  • Porter's Five Forces 분석

제11장 세계 시장 : 모드별

  • 세계의 인하우스 시장 : 지역별
  • 세계의 아웃소싱 시장 : 지역별

제12장 세계 시장 : 스테이지별

  • 세계의 지속적 프로세스 검증 시장 : 지역별
  • 세계의 프로세스 적격성 평가 시장 : 지역별
  • 세계의 프로세스 설계 시장 : 지역별

제13장 세계 시장 : 시험 유형별

  • 세계의 바이오프로세스 잔류물 시험 시장 : 지역별
  • 세계의 추출물 및 침출물 시험 시장 : 지역별
  • 세계의 바이러스 클리어런스 시험 시장 : 지역별
  • 세계의 무선 및 IoT 침입 시험 시장 : 지역별
  • 세계의 기타 시험 유형 시장 : 지역별

제14장 세계 시장 : 지역별

  • 북미
  • 시장에 영향을 미치는 주요 요인
    • 북미의 시장 : 국가별
      • 미국
      • 캐나다
      • 멕시코
      • 기타 북미 지역
  • 유럽
  • 시장에 영향을 미치는 주요 요인
    • 유럽의 시장 : 국가별
      • 독일
      • 영국
      • 프랑스
      • 러시아
      • 스페인
      • 이탈리아
      • 기타 유럽 지역
  • 아시아태평양
  • 시장에 영향을 미치는 주요 요인
    • 아시아태평양의 시장 : 국가별
      • 중국
      • 일본
      • 인도
      • 한국
      • 싱가포르
      • 말레이시아
      • 기타 아시아태평양
  • 라틴아메리카·중동 및 아프리카
  • 시장에 영향을 미치는 주요 요인
    • 라틴아메리카·중동 및 아프리카의 시장 : 국가별
      • 브라질
      • 아르헨티나
      • 아랍에미리트
      • 사우디아라비아
      • 남아프리카공화국
      • 나이지리아
      • 기타 라틴아메리카·중동 및 아프리카 지역

제15장 기업 개요

  • Merck KGaA
  • Thermo Fisher Scientific, Inc
  • SGS SA
  • Eurofins Scientific SE
  • Sartorius AG
  • Charles River Laboratories International, Inc
  • Lonza Group Ltd
  • WuXi AppTec Co, Ltd.
  • Danaher Corporation
  • Cobetter Filtration equipment Co, Ltd.

제16장 바이오프로세스 밸리데이션 시장의 성공 필수 조건

KSA

The Global Bioprocess Validation Market size is expected to reach USD 994.02 million by 2032, rising at a market growth of 8.8% CAGR during the forecast period.

Key Highlights:

  • The North America market dominated Global Bioprocess Validation Market in 2024, accounting for a 40.00% revenue share in 2024.
  • The U.S. market is projected to maintain its leadership in North America, reaching a market size of USD 264.19 million by 2032.
  • Among the various Mode, the In house segment dominated the global market, contributing a revenue share of 79.67% in 2024.
  • In terms of Stage, Continued Process Verification segment are expected to lead the global market, with a projected revenue share of 39.15% by 2032.
  • The Bioprocess Residuals Testing emerged as the leading Testing Type in 2024, capturing a 28.13% revenue share, and is projected to retain its dominance during the forecast period.

The global bioprocess validation market has changed from a qualification activity that happens after development to an integrated, lifecycle-driven field that is shaped by regulatory expectations, new technologies, and new biopharmaceuticals. Validation used to focus on static, batch-level checks. Now, it focuses on risk-based approaches, continuous monitoring, and data-driven oversight. New technologies like single-use systems, continuous bioprocessing, and real-time analytics have changed the requirements, making it necessary to validate disposables, extractables, leachables, and modular systems. The FDA and EMA have pushed for lifecycle and risk-based frameworks, while OEMs and service providers are using digital platforms, simulation tools, and process analytical technologies to make validation faster and more proactive. The market is also growing because biopharma companies are expanding in Asia-Pacific and outsourcing is becoming more common. CDMOs and specialized service providers are taking on bigger roles.

Some important trends are digital and continuous validation through predictive modeling, real-time sensors, and cloud-based analytics; full validation for single-use technologies; and more outsourcing to CDMOs and specialized companies. To meet local regulatory needs, top players use strategies like adding validation to hardware offerings, bundling services, and expanding into new areas. The competitive landscape balances large OEMs like Sartorius, Pall, and Thermo Fisher, who use their global reach and integrated solutions to their advantage, with agile, specialized validation providers who compete on speed, flexibility, and niche expertise. As validation becomes more digital, risk-based, and ongoing, companies that combine regulatory credibility with new ideas and scalable service models will be able to stay ahead of the competition in a market that is both growing and fragmented.

Market Share Analysis

COVID 19 Impact Analysis

The COVID-19 pandemic hurt the bioprocess validation market because it messed up global supply chains, delayed transportation, and made it harder to get raw materials and equipment. Lockdowns and social distancing made it harder for people to work, which slowed down validation activities and pushed back product development. Because of the focus on COVID-19 treatments and vaccines, there was less need for validation in other parts of the pharmaceutical industry. Also, because of uncertainty in the economy, companies cut back on their R&D and compliance budgets, which delayed validation projects and made it take longer to get to market. In general, these things caused problems with operations, lower sales, and a slower growth rate for the market during the pandemic. Thus, the COVID-19 pandemic had a negative impact on the market.

Stage Outlook

Based on Stage, the market is segmented into Continued Process Verification, Process Qualification, and Process Design. The process qualification segment recorded 31% revenue share in the bioprocess validation market in 2024. This stage focuses on demonstrating that bioprocess equipment, systems, and utilities consistently perform within predefined acceptance criteria. It is a critical step in bridging the gap between process design and large-scale production, ensuring that the established parameters hold true under operational conditions.

Testing Type Outlook

Based on Testing Type, the market is segmented into Bioprocess Residuals Testing, Extractables & Leachables Testing, Viral Clearance Testing, Wireless and IoT Penetration Testing, and Other Testing Type. The extractables & leachables testing segment acquired 25% revenue share in the bioprocess validation market in 2024. The increased reliance on single-use systems, disposable bioreactors, polymer-based tubing, and packaging materials in modern biomanufacturing has heightened concerns about potentially harmful substances leaching into final products.

Regional Outlook

Region-wise, the bioprocess validation market is analyzed across North America, Europe, Asia Pacific, and LAMEA. The North America segment recorded 40% revenue share in the bioprocess validation market in 2024. North America and Europe have the biggest share of the global bioprocess validation market because their biopharmaceutical industries are well-established, their regulatory frameworks are strict, and their manufacturing infrastructure is advanced. The United States is the leader in North America because it has strong FDA oversight, a lot of biopharma companies, and a lot of money going into new treatments like monoclonal antibodies, vaccines, and cell and gene therapies. With the help of the EMA's lifecycle-based validation guidelines, Europe has become a center for regulatory-driven innovation. Countries like Germany, Switzerland, and the UK have major biopharma clusters. Both areas put a lot of emphasis on compliance, risk-based validation, and continuous monitoring. This makes there a lot of need for advanced validation services and digital tools that work together.

Asia-Pacific and LAMEA (not including Mexico) are becoming high-growth areas because biologics manufacturing is growing and there is more focus on quality in regulations. Countries in Asia-Pacific, such as China, India, South Korea, and Japan, are putting a lot of money into biomanufacturing capacity. This is increasing the need for validation of single-use systems, continuous processing, and outsourced CDMO services. In LAMEA, on the other hand, Brazil, Saudi Arabia, the UAE, and South Africa are gradually strengthening their biopharma sectors with the help of government programs that aim to diversify healthcare manufacturing. These areas are relying more and more on outside validation providers to meet global standards, which gives both multinational OEMs and regional specialists chances to grow their businesses.

Recent Strategies Deployed in the Market

  • Jul-2025: Sartorius AG teamed up with Sensible Biotechnologies to scale up Sensible's cell-based mRNA platform. The collaboration supports process development, GMP-compliant facility design, and global expansion, enabling clinical-grade production by 2026. This collaboration aims to advance high-quality, scalable mRNA therapeutics with superior purity and performance.
  • Apr-2025: Sartorius AG announced the partnership with Mabion, providing end-to-end biopharmaceutical services from lab-scale development to large-scale manufacturing. The partnership integrates Sartorius' cell line and upstream expertise with Mabion's downstream optimization, validation, and GMP production, enabling faster, high-quality biologics development and streamlined access from DNA to commercial drug products.
  • Dec-2024: Sartorius AG announced the establishment of is Center for Bioprocess Innovation in Marlborough, MA, offering advanced process development, optimization, and validation services. The 63,000 sq. ft. facility supports collaboration with customers and partners, accelerating novel manufacturing processes for cell and gene therapies, and will feature GMP suites for early-stage clinical production.
  • Jun-2024: Thermo Fisher Scientific, Inc. unveiled biobased solutions for single-use bioprocessing containers, reducing carbon emissions in biologics manufacturing. Leveraging plant-based films certified by ISCC PLUS, these innovations maintain product consistency while supporting sustainability. The initiative also includes recycling programs, helping biopharma companies achieve environmental goals without compromising quality or efficiency.
  • May-2024: Sartorius AG announced the partnership with Sanofi to co-develop an integrated continuous biomanufacturing (ICB) platform, enhancing downstream efficiency. Sartorius will leverage its hardware, consumables, and automation, while Sanofi provides R&D support. The platform integrates multiple unit operations, reduces resource use, and improves productivity, aiming to streamline global biologics manufacturing.

List of Key Companies Profiled

  • Merck KGaA
  • Thermo Fisher Scientific, Inc.
  • SGS S.A.
  • Eurofins Scientific SE
  • Sartorius AG
  • Charles River Laboratories International, Inc.
  • Lonza Group Ltd.
  • WuXi AppTec Co., Ltd.
  • Danaher Corporation
  • Cobetter Filtration equipment Co., Ltd.

Global Bioprocess Validation Market Report Segmentation

By Mode

  • In house
  • Outsourced

By Stage

  • Continued Process Verification
  • Process Qualification
  • Process Design

By Testing Type

  • Bioprocess Residuals Testing
  • Extractables & Leachables Testing
  • Viral Clearance Testing
  • Wireless and IoT Penetration Testing
  • Other Testing Type

By Geography

  • North America
    • US
    • Canada
    • Mexico
    • Rest of North America
  • Europe
    • Germany
    • UK
    • France
    • Russia
    • Spain
    • Italy
    • Rest of Europe
  • Asia Pacific
    • China
    • Japan
    • India
    • South Korea
    • Singapore
    • Malaysia
    • Rest of Asia Pacific
  • LAMEA
    • Brazil
    • Argentina
    • UAE
    • Saudi Arabia
    • South Africa
    • Nigeria
    • Rest of LAMEA

Table of Contents

Chapter 1. Market Scope & Methodology

  • 1.1 Market Definition
  • 1.2 Objectives
  • 1.3 Market Scope
  • 1.4 Segmentation
    • 1.4.1 Global Bioprocess Validation Market, by Mode
    • 1.4.2 Global Bioprocess Validation Market, by Stage
    • 1.4.3 Global Bioprocess Validation Market, by Testing Type
    • 1.4.4 Global Bioprocess Validation Market, by Geography
  • 1.5 Methodology for the research

Chapter 2. Market at a Glance

  • 2.1 Key Highlights

Chapter 3. Market Overview

  • 3.1 Introduction
    • 3.1.1 Overview
      • 3.1.1.1 Market Composition and Scenario
  • 3.2 Key Factors Impacting the Market
    • 3.2.1 Market Drivers
    • 3.2.2 Market Restraints
    • 3.2.3 Market Opportunities
    • 3.2.4 Market Challenges

Chapter 4. Market Trends - Bioprocess Validation Market

Chapter 5. State of Competition - Bioprocess Validation Market

Chapter 6. Value Chain Analysis of Bioprocess Validation Market

Chapter 7. Product Life Cycle - Bioprocess Validation Market

Chapter 8. Market Consolidation - Bioprocess Validation Market

Chapter 9. Key Customer Criteria - Bioprocess Validation Market

Chapter 10. Competition Analysis - Global

  • 10.1 Market Share Analysis, 2024
  • 10.2 Recent Strategies Deployed in Bioprocess Validation Market
  • 10.3 Porter Five Forces Analysis

Chapter 11. Global Bioprocess Validation Market by Mode

  • 11.1 Global In house Market by Region
  • 11.2 Global Outsourced Market by Region

Chapter 12. Global Bioprocess Validation Market by Stage

  • 12.1 Global Continued Process Verification Market by Region
  • 12.2 Global Process Qualification Market by Region
  • 12.3 Global Process Design Market by Region

Chapter 13. Global Bioprocess Validation Market by Testing Type

  • 13.1 Global Bioprocess Residuals Testing Market by Region
  • 13.2 Global Extractables & Leachables Testing Market by Region
  • 13.3 Global Viral Clearance Testing Market by Region
  • 13.4 Global Wireless and IoT Penetration Testing Market by Region
  • 13.5 Global Other Testing Type Market by Region

Chapter 14. Global Bioprocess Validation Market by Region

  • 14.1 North America Bioprocess Validation Market
  • 14.2 Key Factors Impacting the Market
    • 14.2.1 Market Drivers
    • 14.2.2 Market Restraints
    • 14.2.3 Market Opportunities
    • 14.2.4 Market Challenges
    • 14.2.5 Market Trends - North America Bioprocess Validation Market
    • 14.2.6 State of Competition - North America Bioprocess Validation Market
    • 14.2.7 North America Bioprocess Validation Market by Mode
      • 14.2.7.1 North America In house Market by Region
      • 14.2.7.2 North America Outsourced Market by Region
    • 14.2.8 North America Bioprocess Validation Market by Stage
      • 14.2.8.1 North America Continued Process Verification Market by Country
      • 14.2.8.2 North America Process Qualification Market by Country
      • 14.2.8.3 North America Process Design Market by Country
    • 14.2.9 North America Bioprocess Validation Market by Testing Type
      • 14.2.9.1 North America Bioprocess Residuals Testing Market by Country
      • 14.2.9.2 North America Extractables & Leachables Testing Market by Country
      • 14.2.9.3 North America Viral Clearance Testing Market by Country
      • 14.2.9.4 North America Wireless and IoT Penetration Testing Market by Country
      • 14.2.9.5 North America Other Testing Type Market by Country
    • 14.2.10 North America Bioprocess Validation Market by Country
      • 14.2.10.1 US Bioprocess Validation Market
        • 14.2.10.1.1 US Bioprocess Validation Market by Mode
        • 14.2.10.1.2 US Bioprocess Validation Market by Stage
        • 14.2.10.1.3 US Bioprocess Validation Market by Testing Type
      • 14.2.10.2 Canada Bioprocess Validation Market
        • 14.2.10.2.1 Canada Bioprocess Validation Market by Mode
        • 14.2.10.2.2 Canada Bioprocess Validation Market by Stage
        • 14.2.10.2.3 Canada Bioprocess Validation Market by Testing Type
      • 14.2.10.3 Mexico Bioprocess Validation Market
        • 14.2.10.3.1 Mexico Bioprocess Validation Market by Mode
        • 14.2.10.3.2 Mexico Bioprocess Validation Market by Stage
        • 14.2.10.3.3 Mexico Bioprocess Validation Market by Testing Type
      • 14.2.10.4 Rest of North America Bioprocess Validation Market
        • 14.2.10.4.1 Rest of North America Bioprocess Validation Market by Mode
        • 14.2.10.4.2 Rest of North America Bioprocess Validation Market by Stage
        • 14.2.10.4.3 Rest of North America Bioprocess Validation Market by Testing Type
  • 14.3 Europe Bioprocess Validation Market
  • 14.4 Key Factors Impacting the Market
    • 14.4.1 Market Drivers
    • 14.4.2 Market Restraints
    • 14.4.3 Market Opportunities
    • 14.4.4 Market Challenges
    • 14.4.5 Market Trends - Europe Bioprocess Validation Market
    • 14.4.6 State of Competition - Europe Bioprocess Validation Market
    • 14.4.7 Europe Bioprocess Validation Market by Mode
      • 14.4.7.1 Europe In house Market by Country
      • 14.4.7.2 Europe Outsourced Market by Country
    • 14.4.8 Europe Bioprocess Validation Market by Stage
      • 14.4.8.1 Europe Continued Process Verification Market by Country
      • 14.4.8.2 Europe Process Qualification Market by Country
      • 14.4.8.3 Europe Process Design Market by Country
    • 14.4.9 Europe Bioprocess Validation Market by Testing Type
      • 14.4.9.1 Europe Bioprocess Residuals Testing Market by Country
      • 14.4.9.2 Europe Extractables & Leachables Testing Market by Country
      • 14.4.9.3 Europe Viral Clearance Testing Market by Country
      • 14.4.9.4 Europe Wireless and IoT Penetration Testing Market by Country
      • 14.4.9.5 Europe Other Testing Type Market by Country
    • 14.4.10 Europe Bioprocess Validation Market by Country
      • 14.4.10.1 Germany Bioprocess Validation Market
        • 14.4.10.1.1 Germany Bioprocess Validation Market by Mode
        • 14.4.10.1.2 Germany Bioprocess Validation Market by Stage
        • 14.4.10.1.3 Germany Bioprocess Validation Market by Testing Type
      • 14.4.10.2 UK Bioprocess Validation Market
        • 14.4.10.2.1 UK Bioprocess Validation Market by Mode
        • 14.4.10.2.2 UK Bioprocess Validation Market by Stage
        • 14.4.10.2.3 UK Bioprocess Validation Market by Testing Type
      • 14.4.10.3 France Bioprocess Validation Market
        • 14.4.10.3.1 France Bioprocess Validation Market by Mode
        • 14.4.10.3.2 France Bioprocess Validation Market by Stage
        • 14.4.10.3.3 France Bioprocess Validation Market by Testing Type
      • 14.4.10.4 Russia Bioprocess Validation Market
        • 14.4.10.4.1 Russia Bioprocess Validation Market by Mode
        • 14.4.10.4.2 Russia Bioprocess Validation Market by Stage
        • 14.4.10.4.3 Russia Bioprocess Validation Market by Testing Type
      • 14.4.10.5 Spain Bioprocess Validation Market
        • 14.4.10.5.1 Spain Bioprocess Validation Market by Mode
        • 14.4.10.5.2 Spain Bioprocess Validation Market by Stage
        • 14.4.10.5.3 Spain Bioprocess Validation Market by Testing Type
      • 14.4.10.6 Italy Bioprocess Validation Market
        • 14.4.10.6.1 Italy Bioprocess Validation Market by Mode
        • 14.4.10.6.2 Italy Bioprocess Validation Market by Stage
        • 14.4.10.6.3 Italy Bioprocess Validation Market by Testing Type
      • 14.4.10.7 Rest of Europe Bioprocess Validation Market
        • 14.4.10.7.1 Rest of Europe Bioprocess Validation Market by Mode
        • 14.4.10.7.2 Rest of Europe Bioprocess Validation Market by Stage
        • 14.4.10.7.3 Rest of Europe Bioprocess Validation Market by Testing Type
  • 14.5 Asia Pacific Bioprocess Validation Market
  • 14.6 Key Factors Impacting the Market
    • 14.6.1 Market Drivers
    • 14.6.2 Market Restraints
    • 14.6.3 Market Opportunities
    • 14.6.4 Market Challenges
    • 14.6.5 Market Trends - Asia Pacific Bioprocess Validation Market
    • 14.6.6 State of Competition - Asia Pacific Bioprocess Validation Market
    • 14.6.7 Asia Pacific Bioprocess Validation Market by Mode
      • 14.6.7.1 Asia Pacific In house Market by Country
      • 14.6.7.2 Asia Pacific Outsourced Market by Country
    • 14.6.8 Asia Pacific Bioprocess Validation Market by Stage
      • 14.6.8.1 Asia Pacific Continued Process Verification Market by Country
      • 14.6.8.2 Asia Pacific Process Qualification Market by Country
      • 14.6.8.3 Asia Pacific Process Design Market by Country
    • 14.6.9 Asia Pacific Bioprocess Validation Market by Testing Type
      • 14.6.9.1 Asia Pacific Bioprocess Residuals Testing Market by Country
      • 14.6.9.2 Asia Pacific Extractables & Leachables Testing Market by Country
      • 14.6.9.3 Asia Pacific Viral Clearance Testing Market by Country
      • 14.6.9.4 Asia Pacific Wireless and IoT Penetration Testing Market by Country
      • 14.6.9.5 Asia Pacific Other Testing Type Market by Country
    • 14.6.10 Asia Pacific Bioprocess Validation Market by Country
      • 14.6.10.1 China Bioprocess Validation Market
        • 14.6.10.1.1 China Bioprocess Validation Market by Mode
        • 14.6.10.1.2 China Bioprocess Validation Market by Stage
        • 14.6.10.1.3 China Bioprocess Validation Market by Testing Type
      • 14.6.10.2 Japan Bioprocess Validation Market
        • 14.6.10.2.1 Japan Bioprocess Validation Market by Mode
        • 14.6.10.2.2 Japan Bioprocess Validation Market by Stage
        • 14.6.10.2.3 Japan Bioprocess Validation Market by Testing Type
      • 14.6.10.3 India Bioprocess Validation Market
        • 14.6.10.3.1 India Bioprocess Validation Market by Mode
        • 14.6.10.3.2 India Bioprocess Validation Market by Stage
        • 14.6.10.3.3 India Bioprocess Validation Market by Testing Type
      • 14.6.10.4 South Korea Bioprocess Validation Market
        • 14.6.10.4.1 South Korea Bioprocess Validation Market by Mode
        • 14.6.10.4.2 South Korea Bioprocess Validation Market by Stage
        • 14.6.10.4.3 South Korea Bioprocess Validation Market by Testing Type
      • 14.6.10.5 Singapore Bioprocess Validation Market
        • 14.6.10.5.1 Singapore Bioprocess Validation Market by Mode
        • 14.6.10.5.2 Singapore Bioprocess Validation Market by Stage
        • 14.6.10.5.3 Singapore Bioprocess Validation Market by Testing Type
      • 14.6.10.6 Malaysia Bioprocess Validation Market
        • 14.6.10.6.1 Malaysia Bioprocess Validation Market by Mode
        • 14.6.10.6.2 Malaysia Bioprocess Validation Market by Stage
        • 14.6.10.6.3 Malaysia Bioprocess Validation Market by Testing Type
      • 14.6.10.7 Rest of Asia Pacific Bioprocess Validation Market
        • 14.6.10.7.1 Rest of Asia Pacific Bioprocess Validation Market by Mode
        • 14.6.10.7.2 Rest of Asia Pacific Bioprocess Validation Market by Stage
        • 14.6.10.7.3 Rest of Asia Pacific Bioprocess Validation Market by Testing Type
  • 14.7 LAMEA Bioprocess Validation Market
  • 14.8 Key Factors Impacting the Market
    • 14.8.1 Market Drivers
    • 14.8.2 Market Restraints
    • 14.8.3 Market Opportunities
    • 14.8.4 Market Challenges
    • 14.8.5 Market Trends - LAMEA Bioprocess Validation Market
    • 14.8.6 State of Competition - LAMEA Bioprocess Validation Market
    • 14.8.7 LAMEA Bioprocess Validation Market by Mode
      • 14.8.7.1 LAMEA In house Market by Country
      • 14.8.7.2 LAMEA Outsourced Market by Country
    • 14.8.8 LAMEA Bioprocess Validation Market by Stage
      • 14.8.8.1 LAMEA Continued Process Verification Market by Country
      • 14.8.8.2 LAMEA Process Qualification Market by Country
      • 14.8.8.3 LAMEA Process Design Market by Country
    • 14.8.9 LAMEA Bioprocess Validation Market by Testing Type
      • 14.8.9.1 LAMEA Bioprocess Residuals Testing Market by Country
      • 14.8.9.2 LAMEA Extractables & Leachables Testing Market by Country
      • 14.8.9.3 LAMEA Viral Clearance Testing Market by Country
      • 14.8.9.4 LAMEA Wireless and IoT Penetration Testing Market by Country
      • 14.8.9.5 LAMEA Other Testing Type Market by Country
    • 14.8.10 LAMEA Bioprocess Validation Market by Country
      • 14.8.10.1 Brazil Bioprocess Validation Market
        • 14.8.10.1.1 Brazil Bioprocess Validation Market by Mode
        • 14.8.10.1.2 Brazil Bioprocess Validation Market by Stage
        • 14.8.10.1.3 Brazil Bioprocess Validation Market by Testing Type
      • 14.8.10.2 Argentina Bioprocess Validation Market
        • 14.8.10.2.1 Argentina Bioprocess Validation Market by Mode
        • 14.8.10.2.2 Argentina Bioprocess Validation Market by Stage
        • 14.8.10.2.3 Argentina Bioprocess Validation Market by Testing Type
      • 14.8.10.3 UAE Bioprocess Validation Market
        • 14.8.10.3.1 UAE Bioprocess Validation Market by Mode
        • 14.8.10.3.2 UAE Bioprocess Validation Market by Stage
        • 14.8.10.3.3 UAE Bioprocess Validation Market by Testing Type
      • 14.8.10.4 Saudi Arabia Bioprocess Validation Market
        • 14.8.10.4.1 Saudi Arabia Bioprocess Validation Market by Mode
        • 14.8.10.4.2 Saudi Arabia Bioprocess Validation Market by Stage
        • 14.8.10.4.3 Saudi Arabia Bioprocess Validation Market by Testing Type
      • 14.8.10.5 South Africa Bioprocess Validation Market
        • 14.8.10.5.1 South Africa Bioprocess Validation Market by Mode
        • 14.8.10.5.2 South Africa Bioprocess Validation Market by Stage
        • 14.8.10.5.3 South Africa Bioprocess Validation Market by Testing Type
      • 14.8.10.6 Nigeria Bioprocess Validation Market
        • 14.8.10.6.1 Nigeria Bioprocess Validation Market by Mode
        • 14.8.10.6.2 Nigeria Bioprocess Validation Market by Stage
        • 14.8.10.6.3 Nigeria Bioprocess Validation Market by Testing Type
      • 14.8.10.7 Rest of LAMEA Bioprocess Validation Market
        • 14.8.10.7.1 Rest of LAMEA Bioprocess Validation Market by Mode
        • 14.8.10.7.2 Rest of LAMEA Bioprocess Validation Market by Stage
        • 14.8.10.7.3 Rest of LAMEA Bioprocess Validation Market by Testing Type

Chapter 15. Company Profiles

  • 15.1 Merck KGaA
    • 15.1.1 Company Overview
    • 15.1.2 Financial Analysis
    • 15.1.3 Segmental and Regional Analysis
    • 15.1.4 Research & Development Expenses
    • 15.1.5 Recent strategies and developments:
      • 15.1.5.1 Partnerships, Collaborations, and Agreements:
    • 15.1.6 SWOT Analysis
  • 15.2 Thermo Fisher Scientific, Inc.
    • 15.2.1 Company Overview
    • 15.2.2 Financial Analysis
    • 15.2.3 Segmental and Regional Analysis
    • 15.2.4 Research & Development Expenses
    • 15.2.5 Recent strategies and developments:
      • 15.2.5.1 Product Launches and Product Expansions:
    • 15.2.6 SWOT Analysis
  • 15.3 SGS S.A.
    • 15.3.1 Company Overview
    • 15.3.2 Financial Analysis
    • 15.3.3 Segmental and Regional Analysis
    • 15.3.4 SWOT Analysis
  • 15.4 Eurofins Scientific SE
    • 15.4.1 Company Overview
    • 15.4.2 Financial Analysis
    • 15.4.3 Regional Analysis
    • 15.4.4 SWOT Analysis
  • 15.5 Sartorius AG
    • 15.5.1 Company Overview
    • 15.5.2 Financial Analysis
    • 15.5.3 Segmental and Regional Analysis
    • 15.5.4 Research & Development Expenses
    • 15.5.5 Recent strategies and developments:
      • 15.5.5.1 Partnerships, Collaborations, and Agreements:
      • 15.5.5.2 Geographical Expansions:
    • 15.5.6 SWOT Analysis
  • 15.6 Charles River Laboratories International, Inc.
    • 15.6.1 Company Overview
    • 15.6.2 Financial Analysis
    • 15.6.3 Segmental and Regional Analysis
    • 15.6.4 SWOT Analysis
  • 15.7 Lonza Group Ltd.
    • 15.7.1 Company Overview
    • 15.7.2 inancial Analysis
    • 15.7.3 Segmental and Regional Analysis
    • 15.7.4 Research & Development Expenses
    • 15.7.5 Recent strategies and developments:
      • 15.7.5.1 Product Launches and Product Expansions:
    • 15.7.6 SWOT Analysis
  • 15.8 WuXi AppTec Co., Ltd.
    • 15.8.1 Company Overview
    • 15.8.2 Financial Analysis
    • 15.8.3 Segmental Analysis
    • 15.8.4 Research & Development Expenses
  • 15.9 Danaher Corporation
    • 15.9.1 Company Overview
    • 15.9.2 Financial Analysis
    • 15.9.3 Segmental and Regional Analysis
    • 15.9.4 Research & Development Expense
    • 15.9.5 SWOT Analysis
  • 15.10. Cobetter Filtration equipment Co., Ltd.
    • 15.10.1 Company Overview

Chapter 16. Winning Imperatives of Bioprocess Validation Market

샘플 요청 목록
0 건의 상품을 선택 중
목록 보기
전체삭제