As EU supplier risk assessment deadlines approach, a number of voluntary third-party auditing and certification options are available. Will more excipient suppliers, and drug manufacturers, use
them?
Certifying Excipient cGMPs
Sep 08, 2015
By Agnes Shanley [1]
Pharmaceutical Technology
Volume 39, Issue 18, pg s14-s18
By Agnes Shanley [1]
Pharmaceutical Technology
Volume 39, Issue 18, pg s14-s18