22. November 2017

Regulators require excipient users to qualify their suppliers based on GMP/GDP audits and they have indicated that third party auditing of suppliers is acceptable if a creditable certification body issues certificates and audit reports by employing qualified auditors who are demonstrably credible in suitable GMP/GDP standards and in the needs of the pharmaceutical industry

30. April 2015

Maxine Fritz — Executive Vice President of Pharma Biotech Consulting at NSF Health Sciences FDANEWS Webinar Wednesday, May 27, 2015 • 1:30 p.m. - 3:00 p.m. EDT http://www.fdanews.com/newgmpstandards