Description

This program is designed to address issues and best practices related to the set of records and procedures that ensure the reliability and integrity of data generated in non-clinical studies, typically used to support regulatory submissions for pharmaceuticals, chemicals, and other regulated products. This documentation is crucial for demonstrating compliance with Good Laboratory Practice (GLP) regulations, which are essential for regulatory acceptance of research findings. The training will cover various aspects, including study protocols, data collection and analysis, record-keeping, and quality assurance procedures.

For Whom: Chief/Senior Laboratory Scientists, Technicians, Quality Control Analysts and Lab Managers.