Live webinar on Preclinical studies regulatory requirements and principle of Good Laboratory Practices (GLP) 2012
09 Oct 2012
Webinar
Description
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
Past Events
Live webinar on Preclinical studies regulatory requirements and principle of Good Laboratory Practices (GLP) 2012 - 09 Oct 2012, Webinar (33102)
Important
Please, check "Live webinar on Preclinical studies regulatory requirements and principle of Good Laboratory Practices (GLP)" official website for possible changes, before making any traveling arrangements
