Validation of Analytical Methods according to the New FDA Guidance

Expired
Dates : 12 April 2017 » 12 April 2017

Place : GRC Training Solutions
United States

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Organizer : david

Topic : Health and Medicine;  FDA compliance, FDA Regulations Training, Regu
Engineering and Technology; Health and Medicine;
Keywords: Design, Health
Description :

Description:

FDA has released a new comprehensive guidance for validation of analytical methods. The guidance follows the modern integrated lifecycle approach with related new requirements for using quality-by-design components, risk assessment, design space and continuous improvement. The guidance will significantly change the way how FDA regulated methods will be developed, validated and used. Because of the novelty of some of the concepts the industry has difficulties to understand and implement the guidance. Attendees of this seminar will understand and learn how to implement the new guidance.

Topics
•    Key differences to the existing guidance 
•    Scope and content of the guidance
•    Going through validation parameters, tests, and acceptance criteria
•    Comparison with ICH Q2
•    How to apply the lifecycle management for analytical procedures
•    When and how to periodic review and revalidate methods
•    Analytical method comparability studies for alternative methods
•    Recommendations analytical method transfer studies
•    Development experiments that should be conducted under GMP conditions
•    Application of QbD components: design space, multivariate experiments, risk assessment 

Who will benefit (by Function)
•    QC managers
•    QA managers and personnel 
•    Laboratory managers and supervisors
•    Analysts
•    Regulatory affairs
•    Training departments
•    Documentation department
•    Consultants

Instructor Profile:

Ludwig Huber, Ph.D., is the director of Labcompliance and editor of www.labcompliance.com, the global online resource for validation and compliance. He is the author of the books "Validation and Qualification in Analytical Laboratories" and "Validation of Computerized Analytical and Networked Systems". He has given multiple presentations mainly on GLP/GMP, 21 CFR Part 11 and Validation around the world. This included seminars, workshops and presentations for the US FDA, China CFDA, ISPE, PDA, PIC/S and several other industry organizations and national health care agencies. For more information, please visit Dr.Huber’s website www.ludwig-huber.com

 

For More information

Email: david@grcts.com | Web: www.grcts.com | Tel:+1-248-233-2049

 


Validation of Analytical Methods according to the New FDA Guidance to be held in GRC Training Solutions, United States between 12 April 2017 and 12 April 2017. It is organised by david. It covers specific areas of Health and Medicine such as  FDA compliance, FDA Regulations Training, Regu. Visit the website of the conference for more detailed information or contact the organizer for specific questions.
Add to calendar 2017-04-12 2017-04-12 Europe/London Validation of Analytical Methods according to the New FDA Guidance https://www.sciencedz.net/en/conference/27118-validation-of-analytical-methods-according-to-the-new-fda-guidance GRC Training Solutions - United States david

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