FDA Regulations for Environmental Monitoring (EM) Program 2017

  • 10 Aug 2017
  • Webinar

Description

FDA Regulations for Environmental Monitoring (EM) Program 2017 is a webinar that covers topics such as:

  • Basics of Setting a Robust and Effective EM Program
  • Applicable Regulations
  • Basics of Designing an Effective and Compliant EM Trend Reports
  • Processing a Completed Environmental Monitoring Test Media
  • Corrective and Preventative Action (CAPA)
  • Basics of Designing an Effective and Compliant EM Excursion Program

FDA Regulations for Environmental Monitoring (EM) Program 2017 is intended for:

  • Quality Assurance
  • Quality Control
  • Chemist, Analysts
  • Microbiologist, Facilities
  • Validation
  • Manufacturing
  • Sterility Assurance
  • Engineering
  • Testing Technicians
  • Compliance
  • Raw Materials Manufacturers
  • Environmental Testing Personnel
  • Laboratories
  • Clinical, Research and Development

Past Events

Important

Please, check "FDA Regulations for Environmental Monitoring (EM) Program" official website for possible changes, before making any traveling arrangements

Event Categories

Business: Internal Audit & Compliance, Quality assurance
Education: E-learning, Education Technologies & Methods, Higher education, Training
Government & Global Issues: Law & Regulations
Health & Medicine: Medical device, Medical laboratories, Medical technology

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