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FDA Audit - Responsibilities of the Auditor and Responsibilities of the firm - Webinar (Recorded)

  • Webinar

  • 60 Minutes
  • March 2020
  • NetZealous LLC
  • ID: 4985665
Overview:
The presentation will include the types of audits that could occur.

What happens when you receive an audit off shore vs. within the US. How do you prepare for these audits? What must be done prior to the audit? What happens during the audit? What happens after the audit? How do you respond? What happens differently if a consultant is involved?

Speaker

Courtland Imel is CEO of Ceutical Laboratories. Courtland has provided training to FDA, Health Canada, and state regulatory authorities. Courtland has spoken at AFDO, AFDOSS, MCAFDO, ASQ, SCC, and Bio. Courtland has 35 years of experience in the industry. Courtland is an SME for several organizations and law firms. Courtland worked for M&M Mars, Allergan, ILEX Oncology, Aronex Pharmaceuticals, Mills Biopharmaceuticals, International Isotopes, Avail Medical Products, Carrington Laboratories, and Ceutical Laboratories, Inc. Courtland has assisted in the submissions of 510Ks, PMAs, IND’s, NDAs, ANDAs, IDEs, and more.

Ceutical Labs provides many services including product development, formulation development, analytical testing (chemistry, microbiology, and physical), regulatory submissions, electronic submissions, consulting, training, quality systems, and more.

Who Should Attend

  • Quality
  • Manufacturing
  • Regulatory Affairs
  • QA/QC/RA
  • R&D
  • Supply Chain
  • Purchasing