OECD Principles of GLP

Objective

Preclinical studies are undertaken to identify a lead candidate and to select the best formulation; determine the route, frequency, and duration of exposure; and support clinical trial design. This course provides essential information on the OECD Principles of GLP, test guidelines and requirements by various regulatory authorities while conducting Preclinical studies.

Syllabus

The syllabus includes History and OECD Principles of GLP, GLP Consensus Documents, Guidance Documents for Compliance Monitoring Authorities, Advisory Documents of the Working Group on GLP, Position Papers, Regulatory authorities, Introduction to Toxicology, Toxicology studies, Ecotoxicology studies, Genetic Toxicology studies, Developmental & Reproductive Toxicology studies, OECD test guidelines and Biocompatibility studies.

 

Instructor

Dr. Ramachandra S.G.
Chief Research Scientist
Central Animal Facility

Target Audience

1. Biomedical Research Institutes
2. R&D units
3. Pharmaceutical industries,
4. Contract Research Organizations

Eligibility criteria

BVSc./B.Pharma/MSc./M.Pharma/MVSc.

 

Course Fee

10000 (Excluding 18% GST)

Number of Credits

2:0

Mode of Instruction

Online  with Synchronous mode

Duration

5 Months (JAN-MAY 2024)

Timings of the class

Wednesday (8.00PM to 10.00PM)

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