MedTech I.Q.

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Dietary Supplements CGMPS - 21 CFR 111 Compliance

21 CFR part 111 ("the DS CGMP rule") requires persons who manufacture, package, label, or hold a dietary supplement to establish and follow current good manufacturing practice-the CGMPs.

This is to ensure the quality of the dietary supplement and to ensure that the dietary supplement is packaged and labeled as specified in the master manufacturing record.

This webinar will discuss basic Dietary Supplement CGMP of Part 111 and related requirements, to include:

  • Quality Management System / QA / QC
  • Personnel, Facilities, Equipment
  • Software controls
  • Production and Process Controls
  • Holding and Distribution
  • Complaints and Returns
  • Records

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