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Pharmacovigilance has grown significantly in recent years and its importance in the healthcare system has been recognized worldwide. There are considerable issues which need to be addressed to ensure the safety of medicines and medical devices. Medical professionals play an important role in the global pharmacovigilance system. They require substantial understanding and expertise in the field of drug and device safety which will successfully contribute to this area through early recognition, management, and reporting of the drug and device safety issues. It is important that medical professionals should be formally trained in the pharmacovigilance. They should possess a combination of training and skills in this area.
Cliniminds Program covers the entire spectrum of Drug Safety Physician / Medical Reviewer Role. Following are the key topics:
1. Introduction to Pharmacovigilance
2. Global Pharmacovigilance Regulations
3. Reportability Criteria & Case reports
4. Safety Reporting and Processing ICSR
5. Medical Evaluation of ICSR
6. Aggregate Report Writing
7. Signal Detection & Risk Management
Online, eLearning Webinars, Hands on use of Safety Database & Signal Management Software. Option of learning Oracle Argus.
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
E learning {3 Months without internship)
Distance Learning {3 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
MBBS, MD, MS, DNB
For further assistance please contact 9072632584 / 91 484 421 6666 / 1800 1023 566 (Toll Free)
TOLL FREE : 1800 102 3566