Aseptic manufacturing of pharmaceuticals ends with fill finish into vials, syringes, or cartridges. It’s crucial to minimize the risk of introducing microorganisms into the drug product. Aseptic filling must provide sterility assurance aligned with regulatory authorities such as EMA, FDA, MHRA, NMPA, TGA, and Health Canada. Watch White Raven’s GMP journey.

Ordering your workcell is a great start. How can you get it up and running as quickly as possible and keep it operating smoothly? And how do you handle interactions with regulatory authorities? Check out our suite of qualification, equipment, and regulatory services.
Watch the video to hear from some of our customers.