ICRI – taking India to the pinnacle of clinical research

Duration of course

  • 9 months

Course Curriculum

Module I Drug Development and Discovery
Module II Basic Principles of Clinical Research
Module III Designing Clinical Trials
Module IV Ethical Issue in Clinical Research
Module V ICH-GCP Guidelines
Module VI Informed Consent Process: Protecting Subject Rights
Module VII Role of CRC and CRA in Clinical Trials
Module VIII Protocol Designing
Module IX Pharmacovigilance in Clinical Research
Module X Standard Operating Procedures
Module XI Requirements and Guidelines to Undertake Clinical Trials in India
Module XII Project Management in Clinical Trials


 

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