Analytical methods and procedures should be validated to ensure reliability, consistency and accuracy of analytical data. Compendial methods should be verified to demonstrate the suitability of laboratories to successfully run the method and when methods are transferred between laboratories successful transfer should be demonstrated through testing. In case a laboratory wants to use an alternative method instead of a compendial method, equivalency of the alternative method to the compendial method should be demonstrated.

Method validation recently got highest attention from regulatory agencies and industry task forces. For example, FDA and EMA released guidelines on method validation and transfer, and USP has proposed new approaches chapters for integrated validation, verification and transfer of analytical procedures, for equivalency testing and for statistical evaluation.

This 2-day workshop will give attendees the background to understand the requirements, and even more significantly, it will focus on strategies and provide tools to implement most critical requirements. It will also provide templates and examples to develop inspection ready documentation. Interactive workshop exercises will be dispersed into and between the presentations. About 50% of the total time will be dedicated to practical sessions with real life examples. After the course a variety of tools such as SOPs, validation examples and checklists will be readily available on a dedicated website that can be used to easily implement what attendees have learned in the course.

Learning Objectives:

• Learn about the regulatory background and requirements for validation of analytical methods and procedures
• Learn how to plan, execute and document development and validation of methods developed in-house
• Be able to explain the different requirements for validation, verification and transfer of analytical procedures
• Understand the principles of validating methods developed in-house, verification of compendial methods, transfer of analytical procedures and demonstrating equivalency to compendial methods
• Be able to explain your company’s strategy for method validation, verification, transfer and equivalency testing
• Be able to select test parameters, test conditions and acceptance criteria for different analytical tasks
• Be able to justify and document decisions about revalidation after method changes
• Be able to define and demonstrate FDA and EU compliance to auditors and inspectors
• Be able to develop inspection ready documentation during on-going routine operation
• Understand statistical evaluation of validation test results
• Understanding what questions will be asked during audits and inspections and how to answer them

Handouts/ Bonus Material for Easy Implementation (available as web downloads):

• 70-page primer: Validation of analytical methods (authored by Dr. Ludwig Huber)
• 10 SOPs related to validation, verification, transfer, review and change of analytical methods
• 10 checklists, templates and examples
• Acceptance criteria for different analytical tasks

Who will Benefit:

• QA managers and personnel
• Quality control
• Method development
• Analytical chemists
• Validation specialists
• Laboratory managers and supervisors
• Regulatory affairs
• Training departments
• Documentation departments
• Consultants

Speaker:

Mark Powell
Director, Mark Powell Scientific Limited

Dr Mark Powell is a Fellow of the Royal Society of Chemistry (RSC) with over thirty years’ experience as an analytical chemist. Mark was Honorary Treasurer of the RSC’s Analytical Division and led a working group on continuing professional development until July 2016, when his term of office ended. Between 2003 and 2013, he was the Analytical Development Manager, and later Scientific Manager, of a UK-based contract research organization which specialized in early-stage oral drug development. During this time, he was responsible for method validation, verification and transfer activities, as well as the qualification of laboratory instruments and computerized data systems. In 2013, he set up Mark Powell Scientific Limited, which provides training and consultancy services to pharmaceutical companies. Mark has since enjoyed working with companies of all sizes around the world on a variety of training and consultancy assignments, and has recently co-authored a White Paper on Pharmaceutical Data Integrity for the laboratory supply company VWR.

For Registration - http://www.complianceonline.com/lab-analytical-compendial-method-ich-q2-glp-part11-annex11-qbd-workshop-seminar-training-80407SEM-prdsm?channel=eventbrite

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