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Analytical Test Methods Validation for GxP Laboratory Compliance: FDA, ICH and USP Requirements - Webinar By GlobalCompliancePanel

22 June 2011, Wilmington, United States


Introduction
This Validation training will address the regulatory requirements which apply at the various stages of development, and suggest proven strategies for compliant and phase-appropriate analytical method validation.

As products are developed from R&D through pre-clinical, clinical and commercial phases, the requirements for analytical test method validation also evolve to meet the increasing regulatory requirements. It is important to know when to do what - too much or unnecessary validation is costly and can delay development programs, while insufficient validation can mean rejection of an application.

This seminar will address the regulatory requirements which apply at the various stages of development, and suggest proven strategies for compliant and phase-appropriate analytical method validation. We will cover the FDA, ICH and USP requirements, and illustrate the components of validation and ways to expedite the validation process. We will cover both small molecule test methods and biotechnology assays, and suggested parameters to validate in each case. The documentation associated with test method validation will be reviewed.

Price List:
Live : $245.00
Corporate live : $995.00
Recorded : $295.00
Venue
Online Training Webinars

Online Training Webinars, 1000 N West Street | Suite 1200, Wilmington, 19801, United States

Organised by
GlobalCompliancePanel
Contact information
Mr David Ross
1000 N West Street | Suite 1200, Wilmington, 19801, United States of America
800-447-9407
Contact us by email

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