Preparing for FDA BIMO Inspection and Management 2014

  • 28 May 2014
  • Webinar

Description

Preparing for FDA BIMO Inspection and Management 2014 is a webinar that covers topics such as:

  • Definitions
  • Statutes and Regulations
  • Regulatory Requirements for Compliance
  • FDA Manuals
  • Inspection Types and Categories
  • FDA BIMO Inspection: Scope and Depth
  • Inspection Process
  • Inspection Classification
  • How to Answer Questions
  • Hosting an FDA Inspection
  • Dos and Don`ts Before, During and After FDA Inspection
  • FDA Forms 482 and 483
  • Misconception and Frequent Mistakes
  • Responding to 483: Best Practices
  • Improving Awareness
  • Enforcement Cases
  • Good Business and Employment Practices
  • Exercising Sound Judgment
  • Practical, Actionable and Sustainable Recommendations: Best Practices
  • Transparency, Accountability and Integrity

Preparing for FDA BIMO Inspection and Management 2014 is intended for:

  • VPs
  • CEOs
  • Attorneys
  • Compliance Officers
  • Clinical Affairs
  • Regulatory Affairs
  • R & D
  • Quality Assurance
  • Contractors/Subcontractors
  • Consultants
  • Anyone Interested in the FDA (BIMO) Inspection Process

Past Events

Important

Please, check "Preparing for FDA BIMO Inspection and Management" official website for possible changes, before making any traveling arrangements

Event Categories

Business: Internal Audit & Compliance
Government & Global Issues: Law & Regulations
Health & Medicine: Medical device, Pharma
Technology: Biotechnology

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