FDA Compliant HPLC Qualification and Performance Testing - Recorded Webinar

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Robinson
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Webinar Duration: 75 minutes

RECORDED: Access recorded version only for one participant; unlimited viewing for 6 months (Access information will be emailed 24 hours after the completion of payment)

SPEAKER:

OVERVIEW:
High Performance Liquid Chromatography is the most frequently used analytical tool for pharmaceutical and API testing laboratories. FDA and international agencies require HPLC equipment to be calibrated, qualified and tested to ensure accurate and reliable analytical results. Even though this is well known since long time, laboratories are unsure on what exactly should be tested initially and on an on-going basis.

The main challenge is to do the right testing in the right sequence. Attendees will learn how to develop qualification and test protocols from planning and setting specifications through installation, operational qualification to performance testing and reporting. .

For Easy Implementation, Attendees Will Receive:
- SOP: Qualification of High Performance Liquid Chromatographs
- SOP: Testing of High Performance Liquid Chromatographs

Areas Covered in the Session:
- FDA and equivalent international requirements
- Examples for recent 483s and Warning Letters
- HPLC qualification according to USP
- Calibration/qualification phases: design qualification, installation qualification, operational qualification, performance qualification
- Selecting parameters and acceptance limits for HPLC initial and on-going testing
- Recommended test sequence for highest efficiency
- Approach for existing systems
- Approach for automated systems (incl. firmware/computer systems)
- Requalification after equipment changes (move, repair, firmware upgrade, hardware upgrade)
- Documentation requirements.

Who Will Benefit:
- Laboratory managers and staff
- Analysts in quality control laboratories
- QA managers and personnel
- Regulatory affairs
- Training departments
- Documentation department

SPEAKER PROFILE:
Ludwig Huber Ph.D., is the director and editor of Labcompliance 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, Informa Healthcare". He has given more than 300 presentations mainly on GLP/GMP, 21 CFR Part 11 and Validation around the world. For more information, please visit Dr. Huber’s website www.ludwig-huber.com

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