Designing Effective and Efficient Extractables or Leachables Studies Course: Literature Gap Analysis and Efficient Study Design as Mandated by FDA Guidelines (ON-DEMAND)


Dublin, June 27, 2024 (GLOBE NEWSWIRE) -- The "Designing Effective and Efficient Extractables or Leachables Studies" training has been added to ResearchAndMarkets.com's offering.

Learn the key phases of an extractables and leachables (E/L) study, including literature gap analysis and efficient study design as mandated by FDA guidelines for drug and biologics packaging. Given the heightened scrutiny of biotechnology drug products, optimizing E/L testing is essential for conserving time and resources.

Join our interactive webinar for a comprehensive E/L study overview, explore valuable literature sources for preliminary insights, and discover how to bridge gaps in information to streamline your study design. We'll delve into E/L study procedures, data management, and real-world case studies while addressing common sponsor challenges.

Who Should Attend:

  • Quality Assurance Departments
  • Quality Control Departments
  • Research and Development Departments
  • Regulatory Affairs Departments
  • Manufacturing Departments
  • Engineering Departments
  • Operations Departments
  • Production Departments
  • Product Development Teams (Formulation and Analytical)
  • Marketing Departments
  • Documentation Departments
  • Supply Chain Departments

Key Topics Covered:

  • Understanding the different types of extractable and leachable
  • Why test for Extractables Leachables
  • Challenges presented by E/L studies
  • Sources of E/L information and how to leverage them
  • Testing for Extractables
  • Testing for Leachables
  • Interpretation of the E/L data

Speakers

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.

For more information about this training visit https://www.researchandmarkets.com/r/27wwuy

About ResearchAndMarkets.com
ResearchAndMarkets.com is the world's leading source for international market research reports and market data. We provide you with the latest data on international and regional markets, key industries, the top companies, new products and the latest trends.

 

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