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Market Overview:
The global GMP Protein (E. coli) Contract Manufacturing Market involves the procurement of E. coli cell cultures used for manufacturing of protein therapeutics under strict Good Manufacturing Practices (GMP) guidelines. Proteins manufactured through GMP approved E. coli cell cultures find applications in areas such as biologics drug development and manufacturing. The increasing investment in cell culture-based biologics has augmented the demand for GMP certified E. coli cell cultures for large scale protein production.
The global GMP Protein (E. coli) Contract Manufacturing Market is estimated to be valued at US$ 685.8 Mn in 2023 and is expected to exhibit a CAGR of 9.7% over the forecast period 2023 to 2030, as highlighted in a new report published by Coherent Market Insights.
Market key trends:
One of the key trends driving the growth of GMP Protein (E. coli) Contract Manufacturing Market is the rising popularity of cell culture systems as an alternative to traditional recombinant protein production techniques. Cell culture techniques offer several advantages over conventional methods such as consistency in product quality, higher yields, and scalability. Moreover, development of optimized cell lines and culture media formulations has enhanced E. coli’s capabilities to produce complex therapeutic proteins. This has expanded the applications of E. coli cell cultures in biopharmaceutical manufacturing.
Porter’s Analysis
Threat of new entrants: The requirement of high capital investments and sophisticated technology act as barriers for new players to enter the GMP protein manufacturing market.
Bargaining power of buyers: Large pharmaceutical companies have significant bargaining power due to their large volume requirements. They can negotiate on price and demand flexible contracts.
Bargaining power of suppliers: A few global players dominate the supply of GMP proteins. This gives them significant bargaining power over pharmaceutical companies in terms of pricing and contract terms.
Threat of new substitutes: There are no close substitutes for GMP grade proteins in clinical trials and commercial production. This reduces the threat of substitutes.
Competitive rivalry: The GMP protein contract manufacturing market consists of several global players. Intense competition exists among players to cater to the growing demand.
Key Takeaways
The global GMP Protein (E. coli) Contract Manufacturing Market is expected to witness high growth, exhibiting a CAGR of 9.7% over the forecast period, due to increasing outsourcing of protein manufacturing activities by pharmaceutical companies.
Regionally, North America is expected to dominate the global market during the forecast period. This is attributed to presence of major GMP protein manufacturers and outsourcing activities by pharmaceutical companies in the region. Europe and Asia Pacific are also expected to witness high growth rates owing to expanding biopharmaceutical industries in countries like China, India, and South Korea.
Key players operating in the GMP Protein (E. coli) Contract Manufacturing market are Merck & Co., Inc., Thermo Fisher Scientific Inc., Abcam plc, GenScript, Biomay AG, SOL GROUP, Proteintech Group, Inc., Nordmark Pharma GmbH, Sino Biological, Inc., Abnova Corporation, Eurofins Scientific, Arcline Investment Management LP, Abgenex, Xpress Biologics, Avid Bioservices Inc, Bio-Techne, Northway Biotech, Aldevron, Institut Mérieux, PerkinElmer Inc., Creative BioMart, Profacgen, ProBioGen AG, 53Biologics, Leadgene Biomedical, Inc., Ajinomoto Bio-Pharma, FUJIFILM Diosynth Biotechnologies, Avioq, Inc, Biovian Oy, KBI Biopharma, GTP Bioways, QIAGEN, Suzhou Novoprotein Technology Co., Ltd., ACROBiosystems, Kactus. Major players are focusing on expanding their manufacturing facilities to cater to the growing demand for GMP grade proteins.
*Note:
1. Source: Coherent Market Insights, Public sources, Desk research
2. We have leveraged AI tools to mine information and compile it
