Nitto Avecia Pharma Services is a FDA inspected cGMP contract development and manufacturing organization supporting the pharmaceutical and biopharmaceutical industries from early phase through post-market life cycle management. With a state-of-the-art facility, experienced staff, and robust quality infrastructure, Avecia Pharma delivers client-centric solutions in a timely manner.
Nitto Avecia Pharma Services has a state-of-the-art facility capable of handling an array of unique products. The facility is complemented by a well-trained and knowledgeable staff with a proven track record of developing processes for some of the most sensitive and complex products. Avecia Pharma's manufacturing department produces batches at the highest quality as the team works hand-in-hand with the Formulation and Quality teams as well as other resources to develop the documentation, process flow, material list and equipment recipes needed in the successful transfer from a lab environment into manufacturing.
Nitto Avecia Pharma Services has received licenses for Pharmaceutical Drug and Device Manufacturing by the California Food and Drug Branch in addition to receiving an ISO 13485 certificate for contract manufacturing and formulation of pharmaceutical, biopharmaceutical, and medical device products.