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Comprehensive practical knowledge to the drug development process, regulatory affairs, essential documentation, roles and responsibilities, ethics, monitoring, case report, pharmacovigilance (PV)related issues.
Module 1 | Overview of Clinical Research |
Module 2 | Pharmacology- General Principles |
Module 3 | Introduction, Definition & Methods in Pharmacovigilance |
Module 4 | Essentials Documents in Pharmacovigilance |
Module 5 | Pharmacovigilance Regulations |
Module 6 | Safety Reporting (including Medical Information) and Processing ICSR |
Module 7 | Aggregate reports, Signal detection & Risk Management |
Module 8 | Audits and Inspections |
Module 9 | Advanced Pharmacovigilance & Analytics |
Module 10 | Hands on Training on Case Processing and Report generation. |
Hands on training on software, online live classes/classroom
Online MCQs/Classroom
Post Graduate Diploma would be awarded upon successful completion of the program. Program accredited by Accreditation Council for Clinical Research Education, USA.
Training would be imparted by the fulltime Think I & Cliniminds faculty and visiting experts from the industry.
Life Long
Face to Face {2 Months Full time Classroom+ 03 Months Optional Industry Internship, 6 Months Weekend (Saturday/Sunday) no internship for weekend batch}
E learning {6 Months without internship)
Distance Learning {6 months}
Please contact counsellor for upcoming batch details 91 812 910 0876 / 91 484 421 6666 / 1800 1023 566 (Toll Free)
COURSE FEE
Actual Fee 69000+18% GST
*Inclusive of applicable tax
MD, MS, MBBS, BDS, BHMS, BAMS, BUMS, BPT, B. Pharm, Graduate/Post Graduate Degree in Life Sciences, Pharmacology, Pharmacy, Medical Laboratory, Nursing, Biochemistry, Microbiology, Biotechnology, and all professionals working with Pharmaceutical companies, Clinical Research Organisations and Hospitals.
TOLL FREE : 1800 102 3566