03-Sep-2024 | Zion Market Research
As per Zion Market Research, the global bioprocess validation market in 2023 surpassed USD 374.07 million and is anticipated to be capitalized more than USD 1107.7 Million by 2032, with a CAGR of just more than 12.82% from 2024–2032. High requirement for the outsourcing of bioprocess validation offerings, stringent quality and safety regulations governing testing and certification of product all over the pharmaceutical and biopharmaceutical industries, and regulatory obligations in the healthcare sector to maintain obedience with GMP (Good Manufacturing Practices) are the primary factors boosting the development of the global market.
The major players active in the global bioprocess validation market are SGS S.A., Merck KGaA, Sartorius Stedim Biotech, Eurofins Scientific, Cobetter Filtration Equipments Co., Ltd., Pall Corporation, DOC S.r.l., Toxikon Corporation, Thermo Fisher Scientific, and MEISSNER FILTRATION PRODUCTS, INC.
Extractables/Leachables Testing Services Section To Add Up For The Biggest Market Share In The Forecast Period
The extractables/leachables testing services section is anticipated to rule the global market in the years to come. The huge share of this section can be credited to the rising outsourcing of testing offerings by biopharmaceutical makers; existence of regulatory guidelines and mandates related to the testing of leachables and extractables; the rising risk of adulteration in products; and the rising need for product identity, safety, quality, and purity.
Pharmaceutical Firms Are Expected To Be The Biggest End Users Of The Global Bioprocess Validation Market
Pharmaceutical firms are anticipated to add up for the biggest share of the global bioprocess validation market in the years to come. The huge share of this section can primarily be credited to rising manufacture of biopharmaceuticals and the corresponding rise in the amount of impurities to be identified for, the stringency of regulations and standards associated with the validity and quality of bioprocesses comprised in the manufacturing.
Asia Pacific Market Is Expected To Develop At The Maximum CAGR From 2024 To 2032
The Asia Pacific bioprocess validation market is projected to develop at the maximum CAGR from 2024 to 2032. The rising requirement for outsourcing bioprocess confirmation, increasing biopharmaceutical manufacturing abilities in Asian nations, rising spending by biotechnology and pharmaceutical firms, and increasing life science research precise to biologics are projected to boost the growth of the global market. In addition to this, the rising number of CDMOs & CROs, increasing awareness about the benefits of biopharmaceutical drugs, and the favorable initiatives by the government to market the development of the biotechnology and pharmaceutical industries in different Asia Pacific nations also boost the global market.
Browse the full “Bioprocess Validation Market - By Process Component (Bioreactors and Filter Element), By Test Type (Integrity Testing, Extractables & Leachable, and Microbiology Testing), and By End-User (Biotechnology & Pharmaceutical Companies, and CDMO) - Global Industry Perspective, Comprehensive Analysis, and Forecast, 2024–2032.” Report at https://www.zionmarketresearch.com/toc/bioprocess-validation-market
The global bioprocess validation market is segmented as follows:
By Test Type
By Process Component
By End User
By Region
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