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Implementing a Phase I QMS (Quality Management System)

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Implementation of a Quality Management System (QMS) must be appropriate for the phase of your product development.

If your company is involved in development or manufacturing for drugs, biologics, and/or medical devices, you must ensure compliance with regulatory requirements for managing quality.

MWA Consulting, Inc. will help you understand the important procedures you will need for a Phase I product, and provide recommendations for meeting your compliance needs.

Join us on Wednesday, July 17, 2019,11 AM PST for our global webinar, where we will share knowledge about implementing a Phase I-appropriate QMS, including:

  • Reviewing the Current Regulations for Phase I QMS
  • Identifying Critical SOPs Required for Phase I Products
  • Discussing Pros and Cons of Using Electronic Systems versus Paper
  • Providing Recommendations for Implementing a Compliant Phase I QMS


Dial-in number (US): (712) 770-4010

Access code: 587569#

International dial-in numbers: https://fccdl.in/i/lisa271

Online meeting ID: lisa271

Join the online meeting: https://join.freeconferencecall.com/lisa271

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