Validation of Analytical Methods according to the New FDA Guidance

  • Speaker:Ludwig Huber
  • Duration:75Min
  • Product Code:GRC-90497

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Recorded Session - How it works

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Training CD - How it works

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(For more information about our products contact +1- 248-233-2049)

If you are unable to attend the meeting Live then you can opt in for the Live Recording instead. Access the recording of the webinar for 6 months. Contact our support for any questions. To prepare an invoice to pay by Check or Wire email us at support@grcts.com. 

Description:

FDA has released a new comprehensive guidance for validation of analytical methods. The guidance follows the modern integrated life cycle 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.

Areas we will be Covering: 

  • 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 re-validate 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

Handouts:

  • Standard Operating Procedure - Validation of Analytical Methods
  • Transfer of Analytical Methods
  • Verification of Compendial Methods

Who will benefit:

  • QC managers
  • QA managers and personnel 
  • Laboratory managers and supervisors
  • Analysts
  • Regulatory affairs
  • Training departments
  • Documentation department
  • Consultants

Certifications: GRCTS Attendance Certificate

Instructor Profile:
Ludwig Huber, Ph.D., is the director of Lab Compliance. 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.

Available Options

Recording: 6 Months Access to the Training which can be accessed from any location

$259

CD-DVD: Shipped within 2 working days

$359

USB - Shipped within 2 working days

$389

5 Member Group: 5 people can Attend the Live Online Meeting from any location globally

$2,659

10 Member Group: 10 people can Attend the Live Online Meeting from any location globally

$4,659

Recording Access for 12 Months: Participant can access the training Recording for 12 months from any location

$1,259

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