
The global good manufacturing practice (GMP) standards biologics market is growing rapidly, expected to be valued at around $52.7 billion in 2026 and projected to reach $98.2 billion by 2033, with a compound annual growth rate (CAGR) of 9.3% during the forecast period, according to Persistence Market Research
Growth is being driven by rising demand for monoclonal antibodies (MAbs), recombinant proteins, cell and gene therapies, and biosimilars, alongside increasing outsourcing of biologics manufacturing to contract development and manufacturing organizations (CDMOs). Continuous advances in single-use bioprocessing, automation, continuous manufacturing, and digital quality management systems are enabling manufacturers to improve production efficiency while maintaining strict compliance with US Food and Drug Administration (FDA), European Medicines Agency (EMA), and other global GMP standards.
This article is accessible to registered users, to continue reading please register for free. A free trial will give you access to exclusive features, interviews, round-ups and commentary from the sharpest minds in the pharmaceutical and biotechnology space for a week. If you are already a registered user please login. If your trial has come to an end, you can subscribe here.
Login to your accountTry before you buy
7 day trial access
Become a subscriber
Or £77 per month
The Pharma Letter is an extremely useful and valuable Life Sciences service that brings together a daily update on performance people and products. It’s part of the key information for keeping me informed
Chairman, Sanofi Aventis UK
| Headless Content Management with Blaze