Effective Records Management and Document Control for Medical Devices

Effective Records Management and Document Control for Medical Devices is a webinar that covers topics such as:

  • Description of typical document control system in use
  • QSR and ISO 13485 requirements for document control
  • Establish systems that will speed up review of new or revised documents
  • How to create uniform documentation that is easy to follow
  • Eliminate common formatting problems that create confusion
  • Streamlined document control process
  • Ensure obsolete documents are removed from use
  • Create more control over controlled documents in circulation

Effective Records Management and Document Control for Medical Devices is intended for:

  • Research and Development Departments
  • Quality Assurance Departments
  • Manufacturing Departments
  • Regulatory Affairs Departments
  • Operations Departments
  • Engineering Departments
  • Documentation Departments
  • Production Departments
  • Everyone involved with FDA compliance
  • Executive Management

Important

Please, check the official conference website for possible changes, before you make any traveling arrangements

Prices are for evaluation only.

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