Industry Program in Clinical trials research & Administratio

Clinical Trials is a branch of healthcare science that determines the safety and effectiveness of medications, devices, diagnostic products and treatment regimens intended for human use. These may be used for prevention, treatment, diagnosis or for relieving symptoms of a disease. Clinical Research is different than clinical practice. In clinical practice one uses established treatments, while in clinical research evidence is collected to establish a treatment.

The term clinical research refers to the entire bibliography of a drug/device/biologic, in fact any test article from its inception in the lab to its introduction to the consumer market and beyond. Once the promising candidate or the molecule is identified in the lab, it is subjected to pre-clinical studies or animal studies where different aspects of the test article (including its safety toxicity if applicable and efficacy, if possible at this early stage) are studied.

Course Module Module Name
Paper I Introduction to Clinical Trials
Paper II Contract Research and Clinical Trial Environment
Paper III ICH International Conference of Harmonization
Paper IV ICMR -Guidelines on Biomedical Research on Human Subjects
Paper V Introduction to Clinical Trial Administration
Paper VI Introduction to Clinical Trial Research