For demonstration and documentation of the batch-to-batch consistency of any given biopharmaceutical material, its identity, purity, quantity, bioactivity and profile of impurities must be confirmed.
These tasks are addressed by our portfolio of analytical routine methods for quality control of biopharmaceuticals, and complemented by qualified external partners. Thus, we are able to provide full quality control of biological APIs and clinical samples.
Click on the following links for more information:
Click here for more information.
Advertise With UsAdvertise on our extensive network of industry websites and newsletters.
Get the PBR newsletterSign up to our free email to get all the latest PBR
news.
