FDA Manuals and Inspection Guides
This seminar is intended to discuss what FDA-regulated industry should know about FDAâ€™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 speakerâ€™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 Donâ€™ts before, during and after the inspection.
This presentation will provide great opportunities to become familiar with the FDA inspection policy and industryâ€™s best GMP practices including the lessons learned from the most common deficiencies observed during the FDA inspections of firms (devices and pharmaceuticals) for the past eight years.
Areas To Be Covered in this Seminar:
â€¢ Applicable Laws and Regulations
â€¢ FDA Manuals and Inspection Guides
â€¢ Hosting an FDA Inspection
â€¢ Inspection Types and Categories
â€¢ Inspection Classification
â€¢ FDA Forms 482 and 483
â€¢ Common deficiencies in 483s
â€¢ What/How to Prepare for and Manage an FDA Inspection
â€¢ How to Communicate Before, During and After inspection: Dos and Donâ€™ts
â€¢ Inspection Preparation Procedures
â€¢ Close Out Meeting
â€¢ Responding to 483s, If Issued
â€¢ How to Communicate with Emotional Intelligence
â€¢ Employee Training
â€¢ Actual Case Studies
â€¢ Speakerâ€™s PASS-IT Recommendations.
For More Details:https://www.grcts.com/GRC-90060
Tel:+1-248-233-2049 | Web:www.grcts.com
8 Jan 2017 Plano, TX
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