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Method Validation under Good Laboratory Practices (GLP)

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Refunds up to 30 days before event

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This laboratory compliance training will teach you how to validate an analytical method under the GLP requirements. It will cover in detail the criteria for the validation of an analytical method including statistical and documentation requirements.

Why Should You Attend:

Any laboratory that supports products for sale or use in the United States must follow Good Laboratory Practices (GLP), a comprehensive system that guarantees validity of results. If you work in pharmaceuticals, chemicals and petrochemicals, and environmental analyses then you are mandated to be following GLP. One of the major tasks in GLP is validation of an analytical method. All methods must be validated. Common criteria are accuracy, precision, linearity, range, and several more.

This webinar will teach you how to validate an analytical method under the GLP requirements.

Areas Covered in the Webinar:

  • Method validation
  • The criteria for a method
  • Statistical requirements
  • Documentation requirements
  • Common issues

Who Will Benefit:

This webinar will provide valuable assistance to all personnel working in a GLP certified laboratory and for those developing methods for environmental analysis, chemicals, petroleum products and petrochemicals. Employees who will benefit include:

  • QA Managers
  • QC Managers
  • Analytical Chemists
  • Validation Specialists
  • Laboratory Managers and Supervisors
  • Regulatory Affairs Personnel
  • Documentation Specialists

Instructor Profile:

John Fetzer

John Fetzer
Consultant, Fetzpahs Consulting

John C. Fetzer, has had over 30 year experience in HPLC methods development. He has authored or co-authored over 50 peer-reviewed papers on liquid chromatography, has served on the editorial advisory boards of the Journal of Chromatography, Analytical Chemistry, and Analytical and Bio analytical Chemistry.

Topic Background:

The new pharmaceuticals are very often completely new compounds, structures never studied before by chemists. Their properties – such as solubilities and acid-base nature, are unknown. Synthetic reactions may make many similar types of molecules, including structural and optical isomers. The methodologies that mean US Food and Drug Administration compliance with GLP require a separation to be able to separate and identify all major, minor, and trace components. It is no longer just determining a purity of the main component. Each minor contaminant or degradation product is also important in GLP.


For Registration - http://www.complianceonline.com/method-validation-under-good-laboratory-practices-glp-webinar-training-703561-prdw?channel=eventbrite


Note: Use coupon code REFERRAL10 and get 10% off on registration.

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Date and Time

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Refund Policy

Refunds up to 30 days before event

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