Meet FDA Expectations for a Tougher Supplier Audit Program - Webinar By GlobalCompliancePanel
News and Society
About the Author:
John E. Lincoln is a medical device and regulatory affairs consultant. He has helped companies to implement or modify their GMP systems and procedures, product risk management, U.S. FDA responses. In addition, he has successfully designed, written and run all types of process, equipment and software qualifications/validations, which have passed FDA audit or submission scrutiny, and described in peer-reviewed technical articles, and workshops, world wide. John has also managed ...Read the rest of this entry »
April 26th, 2012



Home