Live webinar on Preclinical studies regulatory requirements and principle of Good Laboratory Practices (GLP) 2012
09 Oct 2012
Webinar
Key Topics
General requirements for preclinical studies
The role of Preclinical/Safety/Tox studies during the drug clinical development and NDA
GLP principles
Who should Attend
Regulatory Affairs
Pharmaceutical development
Research and Development and Quality Assurance & Control
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Important
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