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This webinar will help you better understand test method validations to verify the performance of a Medical Device, global reference standards, the FDA requirements and how to perform successful TMV to ensure your inspection of verification is effective, using detailed real-life case studies.


  • Test Method Validation - Overview
  • Quality System Regulation, 21 CFR Part 820, and ISO 13485 - Overview
  • When should Methods be Validated?
  • Qualification vs Validation
  • Types of Test Method Validations
  • How to perform successful test method validations


Test method validation is an often-confusing requirement for medical devices. A fundamental issue is the role-reversal between the test method and the product or process it is designed to detect. Although the FDA provides guidance on method validation, the Code of Federal Regulations (CFR) Title 21 Part 820: Quality System Regulation (QSR) 21 does not specifically broach the topic of method validation. It alludes to it in equipment qualification, statistical methods, process validation, design controls, and other sections. In numerous warning letters, we have witnessed significant importance of method validation as an applicable medical device validation activity.

Attend this webinar to understand when the method to be validated, validation vs qualification and all FDA requirements of test method validation and most importantly how to perform test method validation and ensure your inspection of verification is effective.


  • How to ensure your inspection of verification is effective
  • Detailing real-life case studies
  • Understanding global reference standards for test method validation
  • FDA requirements for TMV
  • How to prove your inspection method is repeatable and reliable
  • Recommendations: Some Best Practices and Strategies


  • Research & Development
  • Quality Engineers and Auditors
  • Manufacturing Engineers
  • Regulatory Affairs Teams
  • Quality Assurance & Quality Control Teams
  • Operations Teams
  • Document Control
  • Design Assurance Teams
  • Device Development Teams
  • Personnel involved in Verification and Validation planning, execution and documentation for devices
     


José Mora is a Principal Consultant and Project Manager specializing in Manufacturing Engineering, Quality Systems, and Lean Transformations. José is a recognized subject matter expert in process validation, lean manufacturing, lean controlled document systems, startup operations, process development, and quality systems, having lectured internationally and presented webinars on these subjects.

For over 30 years he has worked in the life sciences in positions ranging from Senior Engineer and Project Manager to Vice-President, specializing in manufacturing, process development, tooling, and quality systems. His medical device experience includes surgical instruments, PTA & PTCA dilatation and guiding catheters, plastic surgery implants and tissue expanders, urology implants and devices for the treatment of incontinence, delivery systems for brachytherapy, orthopedic implants and instruments, and vascular surgery grafts and textiles.

Irrespective of the places he worked, Jose has a track record of introducing world-class methodologies such as Kepner-Tregoe, Taguchi techniques, Theory of Constraints, Lean Manufacturing, Five S (Visual Workplace), process validation to Global Harmonization Task Force standards, and similar approaches. He has implemented various good manufacturing practices like JIT, kanban systems, visual workplace, and lean manufacturing practices. He has also published a white paper on the application of lean manufacturing methods to the creation and management of controlled documents and a template for strategic deployment.

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