Live webinar on Preclinical studies regulatory requirements and principle of Good Laboratory Practices (GLP) By compliance2go October 9, 2012

The course will briefly discuss the general preclinical/tox data requirements for the new drug application. The course will also provide understanding of the terminology, regulations and mandated practices for GLP testing and compliance. Special attention will be paid to the critical compliance aspects of gathering pre-clinical data in a regulated environment.

Areas Covered in the Session:

The role of Preclinical/Safety/Tox studies during the drug clinical development and NDA.

General requirements for preclinical studies;

GLP principles.

Webinar Includes:

Get a chance to attend the Q/A Session with the Expert to ask your toughest question

PDF print only copy of PowerPoint slides

60 Minutes Live Presentation

Official Website: https://compliance2go.com/index.php?option=com_training&speakerkey=36&productKey=180