With over 27 years of biologics development experience and 18 years as a CDMO, Avid Bioservices possesses extensive expertise in transitioning molecules through the product life cycle from early development into commercial manufacturing.
Our manufacturing team members are trained to understand the science behind each process. Our experts are committed to your success at every level and every step of the way. Our process development, manufacturing and quality teams partner seamlessly to ensure that operations result in a safe end-product for your patients.
We have extensive experience leading our clients through process validations and have a long commercial manufacturing history working with large pharmaceutical organizations. Since Avid’s inception, we have completed process performance qualification (PPQ) campaigns for 10 client products, two of which obtained regulatory approval and for whom we currently manufacture commercial product. Avid expects pre-approval inspections (PAI) on three of the most recent PPQ campaigns and is ready for commercial product demand should our clients obtain regulatory approval.