Test Article Management and Characterization for Drugs and Devices
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Keywords: Analysis
This 90-minute webinar will clarify your confusion about Test Article Characterization for GLP drug studies. You will learn the correct way to use GMP characterization data in a GLP study, understand how to characterize a medical device as a test article, learn the common mistakes made in test article characterization and the basic requirements for drug and device stability testing.
Why Should You Attend:
The presentation will begin with a review of GLP requirements for test and control article characterization, regardless of whether the article is a drug or device. It will address the study director's responsibilities and sponsor responsibilities in test article characterization. Attendees will learn the best practices for managing GMP characterizations, stability, and certificates of analysis.
Areas Covered in the Seminar:
- What are the recommended procedures for chemical and physical characterization of drugs/devices in safety testing.
- What are the basic requirements of test article characterization.
- How to manage carry-over from test to control article
- How to use GMP test article characterization and the certificate of analysis for a GLP study
- How to define a device test article
- How to characterizing medical devices
Test Article Management and Characterization for Drugs and Devices to be held from 08 junho 2012 to 08 junho 2012 in Online Webinar, Estados Unidos. It covers various areas of Não classificadas including . For more information, visit the website of the conference or contact the organizer.
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