How to withstand an FDA audit of your facilities: A primer for clinical sites, manufacturing facilities and labs

This FDA Audit webinar training will discuss the types of audit and what are the activities to be done before, during and after FDA audit to pass it successfully and how to increase credibility for your company.
Why Should You Attend:
If your company is marketing a product or service that is regulated by the FDA, you should be prepared for an FDA audit. If you have never been audited by the FDA or if you were last audited 4-6 years ago, if any product or service you offer has been in the news – positive or negative, or if you are getting ready to submit a clinical trial or marketing approval application, chances are you would get audited by the FDA in the near future. Although different facilities are subject to different regulations, FDA auditors follow some general guidelines that are common across all.
We will discuss the general rules and specific case studies to highlight the common themes and differences across facilities subject to GCP, GMP or GLP regulations. This webinar will discuss ways to be prepared for an FDA audit, conduct during an audit, and follow-up activities to an audit. Learn how convert an FDA audit into an opportunity to demonstrate high quality products and services, and to increase credibility in the industry for your company.
Areas Covered in the Seminar:

  • Types of FDA audits
  • Key guidelines available from FDA
  • GCP/GMP/GLP requirements. Why inspections are conducted and by what statutory authority?
  • Reasons for FDA conducting an inspection.
  • What to expect from an audit? What is subject to FDA purview and what's off-limits?
  • Preparing for the inspection/Audit - What you need to know and do to prepare for, during and even after the inspection, a ctions to be taken upon the investigator's arrival, required documentation, Individual responsibilities for the inspection.
  • Logistics of the FDA audit/Inspection
  • Follow-up to an FDA audit - What to do next? How to respond to findings and facilitating the documentation and remediation process…and reaching final closure?
  • Do's and don'ts of an FDA audit/Inspection.

Who Will Benefit:
This webinar will provide valuable assistance to all personnel in:

  • QA/QC/Compliance/ Regulatory affairs professionals
  • Senior management executives (CEO, COO, CFO, etc)
  • Manufacturing managers, supervisors & personnel
  • Clinical and preclinical laboratory managers
  • Clinical trial specialists
  • Project Managers
  • People investing in FDA-regulated product development projects

For Registration:
http://www.complianceonline.com/ecommerce/control/trainingFocus/~product_id=701869?channel=biofind
Note: Use this promocode(117660) for 10% discount.