Master Production Record Requirements - Webinar By GlobalCompliancePanel 2011

  • 21 Jun 2011
  • Webinar

Description

Master Production Record Requirements - Webinar By GlobalCompliancePanel 2011 is a webinar that is focused on Roles and Responsibilities, Device Master Record (DMR), Issuance of BPR, Content of the MPR, Review and Approval of MPR, Creation and Revision of Master Production Record (MPR), Regulatory Expectation (FDA and EU).

The event brings together:

  • Maintenance
  • Regulatory Affairs
  • Quality Control
  • Materials Management
  • Validation
  • Quality Assurance
  • Manufacturing



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Important

Please, check "Master Production Record Requirements - Webinar By GlobalCompliancePanel" official website for possible changes, before making any traveling arrangements

Event Categories

Business: Operations, Quality assurance
Education: Training
Government & Global Issues: Law & Regulations
Health & Medicine: Healthcare, Medical technology

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