Andelyn Biosciences Solutions

LOOKING FOR SCALABILITY IN CLINICAL MANUFACTURING?

Andelyn Bioscience’s current Good Manufacturing Practices (cGMP) Clinical Manufacturing Facility operates according to FDA cGMP Guidelines and with multinational health agencies around the world.

The CMF currently consists of a clean room suite with ISO Class 5/7/8 spaces. This space is comprised of five production suites and has the capability to produce up to five different viral vector products simultaneously. The clean room space also includes dedicated areas for solution preparation, cell culture, and fill/finish.