ComplianceOnline

Responding to FDA 483s and FDA Warning Letters - Best Practices

Instructor: Angela Bazigos
Product ID: 702451
Training Level: Basic to Advance
  • Duration: 120 Min

recorded version

$299.00
1x Person - Unlimited viewing for 6 Months
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Recorded Link and Ref. material will be available in My CO Section

Training CD

$499.00
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(For multiple locations contact Customer Care)
CD and Ref. material will be shipped within 15 business days

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Read Frequently Asked Questions

This webinar on responding to FDA 483s and Warning Letters will provide tips for avoiding FDA 483s and warning letters, and train you on the best practices in responding to a 483 or warning letter so that you can manage the consequences of the findings from escalating.

Course "Responding to FDA 483s and FDA Warning Letters - Best Practices" has been pre-approved by RAPS as eligible for up to 2 RAC credits towards a participant's RAC recertification upon full completion.

Why Should You Attend:

Audits by the FDA are perhaps the most intimidating of all events at a regulated facility. Each year, the FDA conducts several thousand audits, approximately half of which lead to findings that result in Form 483s. Most Form 483 audits are amicably resolved, but a few lead to serious consequences for the audited parties, starting with Warning Letters and ending with heavy fines and jail time for a few.

This webinar, will assist you in responding to a 483 or Warning Letter so the consequences of the findings do not escalate beyond the current status.

Areas Covered in the Seminar:

  • FDA Inspections - background.
  • Causes of Form 483 / Warning Letter.
  • Some recent results of companies failing to respond appropriately.
  • Best Practices for Responding to 483.
  • Best Practices for Responding to Warning Letter.
  • What to do if the responses fail.

Who Will Benefit:

  • CEOs
  • Regulatory Affairs professionals
  • Quality
  • IT
  • Engineers
  • Small business owners
  • GxP
  • Consultants

Instructor Profile:

Angela Bazigos, is the CEO of Touchstone Technologies Silicon Valley and has almost 30 years experience in lifescience. She has received a patent for speeding up software compliance and has applied for patents aimed at speeding up software compliance and FDA software audits. She has co-authored “Computerized Systems in Clinical Research” with the FDA, DIA and Academia and teaches classes in project management, computer systems validation, quality assurance and IT. She is the Vice President of the Pacific Regional Chapter of Society of Quality Assurance and writes articles for the SQA journal. She is also a member of DIA, RAPS and CVIC. She was recently inducted into Stanford’s Who’s Who for contributions to the LifeSciences industry.

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