Share Our Information
February 02, 2016
Susan Schniepp, Distinguished Fellow of Regulatory Compliance Associates® Inc., discusses how to create a robust corrective and preventive action (CAPA) system and how to identify root cause.
Complete article published in PharmTech.
Ensure Quality in a Contract Test Laboratory...Read More
FDA Inspections: Hope is Not a Strategy...Read More
Responding to FDA CAPA Requests...Read More