'Sustainable fda inspection' presentation slideshows

FDA Inspection Policy and Best GMP Practices

This seminar is intended to discuss what FDA-regulated industry should know about FDA�s inspection policy to better implement the best Good Manufacturing Practices (GMPs). The common deficiencies found based on 483s issued to medical device and pharmaceutical industries will be discussed. The most common deficiencies are based on the speaker�s analysis of 483s issued for the past eight (8) years. This presentation will greatly help you better prepare for and manage an FDA inspection in a proactive and effective manner.�The speaker will also discuss practical, actionable, and sustainable guidance on how to prepare for a sustainable FDA inspection and how to manage the FDA inspection process including Dos and Don�ts before, during and after the inspection.�

200 views • 6 slides