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GMP for QC Laboratory Compliance

In the manufacture and quality control of medicinal products, compliance with the GMP rules is the decisive aspect of manufacturing high-quality products. For this reason, every staff member in the pharmaceutical industry has to be familiar with the basic GMP requirements.

Webinar Jan 06 2026, Tuesday 01:00 PM EDT 90 Minutes Basic Level Code: GRC0000277
Speaker
By Kelly Thomas In Clinical Trial and Clinical Research
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The Good Manufacturing Practice Program provides a comprehensive overview of the best practices regarding the management of manufacturing and quality control testing for pharmaceutical products.

  • You get to know the most important pharmaceutical regulations and their importance
  • You get a basic overview of GMP requirements in pharmaceutical production, and
  • You become familiar with technical terms from the field of GMP and their meaning
  • Understand the regulatory requirements governing GMP-compliant QC Labs
  • Understand how to apply those requirements
  • Understand the regulatory expectations regarding laboratory design and utilities
  • Understand the regulatory expectations regarding laboratory equipment/instrumentation

  • Analytical Development
  • Quality Assurance
  • Quality Control
  • Validation
  • Regulatory Affairs

Kelly Thomas
Kelly Thomas

Ms. Thomas has over two decades of cGMP hands-on industry experience in both pharmaceutical and medical device manufacturing operations.Her experience covers all Quality Systems; as well as, all areas of validation; including, process/product validation, facilities validation, CSV and 21 CFR Part 11, test method validation, equipment/automated processes and cleaning validation.Utilizing strategic thinking, risk-based approaches, and Lean principles, she has demonstrated success in steering and managing complex projects within the pharmaceutical and medical device industries.

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