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QbD Approach to Analytical Method Lifecycle: Design, Development, Validation and Transfer

 

This training on using the QbD approach to analytical method lifecycle is designed to provide participants with a lifecycle approach to developing and

QbD Approach to Analytical Method Lifecycl Design Development Validation and Transfer

 

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  • 1x Person - Unlimited viewing for 6 Months

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    USD 299
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  • One CD or USB is for usage in one location only

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    USD 399
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  • LIVE + RECORDED VERSION

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  • LIVE + TRAINING CD or USB

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About The Event

QbD Approach to Analytical Method Lifecycle: Design, Development, Validation and Transfer

 
This training on using the QbD approach to analytical method lifecycle is designed to provide participants with a lifecycle approach to developing and validating analytical methods and comply with compendial requirements. The webinar presenter will use case studies to illustrate each stage in the process.

Why Should You Attend:

This webinar is designed to provide participants with a lifecycle approach to developing and validating analytical methods, including some elements aligned with QbD concepts. By using a lifecycle approach, methods are more likely to meet their intended purpose, and scientists are more likely to have success during validation and transfer exercises.

The course will build on traditional concepts of method development, validation and transfer by introducing the Analytical Target Profile (which identifies what the method is expected to accomplish), fostering method understanding (using QbD concepts to explore the method operable region and stressing the importance of real samples in the environment where they will be tested) and demonstrating how these principles can be used iteratively as methods change location or evolve technically. This approach will be linked with current compendial requirements. There will be an opportunity for questions and answers at the end of the presentation.

The webinar instructor, a leading expert on the subject, will use his industry knowledge in presenting relevant case studies to increase participants’ understanding of the three stages of an analytical method lifecycle.

Learning Objectives:

  • Understand the lifecycle approach to method development and validation.
  • Learn more about the three stages of an analytical method lifecycle.
  • Identify an Analytical Target Profile for methods being developed
  • Understand how validation, verification and method transfer are interrelated.
  • Comply with compendial requirements for verification with greater success and fewer resources.

Areas Covered in the Webinar:

  • Introduction: Using a Lifecycle Approach for Analytical Procedures
  • Stage 1: Method Design, Development and Understanding
    • Using an Analytical Target Profile to Guide Development
      • Case study
    • Using QbD Principles to Explore the Method Operable Design Space
      • Case study
  • Stage 2: Method Qualification
    • Integrating Validation, Verification and Transfer
      • Case study
  • Stage 3: Method Performance Verification
    • Using Change Control and Risk Assessment
      • Case study
  • Questions and Discussion

 

Who Will Benefit:

This webinar will provide valuable assistance to personnel in biotech and pharmaceutical companies/manufacturing sites, including:

  • Chemists (research and quality control personnel) involved in analytical method development, validation or transfer
  • Regulatory affairs/CMC personnel responsible for documenting analytical methods and their acceptability
  • Laboratory managers and staff
  • Analysts
  • QA/QCU managers and personnel
  • Training department
  • Documentation department
  • Consultants

Instructor Profile:

Gregory Martin

Gregory Martin
Founder and President, Complectors Consulting LLC

Gregory Martin is president of Complectors Consulting, which provides consulting and training in the area of pharmaceutical analytical chemistry. Mr. Martin has over 25 years’ experience in the pharmaceutical industry and was director of pharmaceutical analytical chemistry (R&D) for a major pharma company for a number of years. In addition, he has volunteered for the USP for over 10 years, and currently serves as vice chair of the General Chapters – Physical Analysis Expert Committee, and serves on expert panels on validation and verification, weights and balances, residual solvents and use of enzymes for dissolution testing of gelatin capsules.

He has particular interest in QbD/Lean approaches to dissolution testing, impurity methods, method lifecycle (development/validation/transfer) and instrument qualification, and is passionate about using good science and sound logic to achieve high quality results, consistent with cGMPs, while minimizing resources. He is also past chair of the AAPS In Vitro Release and Dissolution Testing Focus Group. Mr. Martin is author of several papers in the areas of dissolution and analytical method validation.

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