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GxP 101: Creating a Workable User Requirement Specification (URS) for your Life Science Facility

In this webinar on-demand, you will learn how to set up a URS for your life science facility. Sean Merrill, validation engineer global qualification / validation expert at ELPRO will explain the following topics:

  • Validation and qualification explained as part of a quality management system
  • Guidance for setting up your URS
  • GMP premises, equipment, and calibration considerations
  • Ensuring your facility monitoring is a quality system of record
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