CLINICAL RESEARCH & PHARMACOVIGILANCE
Global Institute of Health Science is a pioneer in health science education especially in distance & online education. Global Institute of Health Science is an ISO 21001:2018 Certified health science Institute & globally acclaimed, also certified with copyright approval from IPR Government of INDIA. GIHS have international certification from UASL UK for Quality Control Management System.
WHY CHOOSE US
GHIS Clinical Research and Pharmacovigilance courses online program is designed to provide total overview and skill globally in the field of clinical research.
It would help professionals to upgrade & develop their knowledge about ICH GCP Guidelines, regulatory issues and other major aspects of clinical research & trial management.
It is designed to provide total overview and skill globally in the field of clinical research, and pharmacovigilance.
It would help professionals to upgrade & develop their knowledge about clinical trials, data management, pharmacovigilance, regulatory issues and other major aspects of pharmacovigilance. to understand the key concepts in the responsible conduct of research and that conforms to the highest standards for the protection of human research subjects. It can be able to critically appraise the medical scientific literature, including the methodology of published and proposed investigations.
SYLLABUS
GHIS Clinical Research and Pharmacovigilance courses online program is designed to provide total overview and skill globally in the field of clinical research. It would help professionals to upgrade & develop their knowledge about ICH GCP Guidelines, regulatory issues and other major aspects of clinical research & trial management. It is designed to provide total overview and skill globally in the field of clinical research, and pharmacovigilance. It would help professionals to upgrade & develop their knowledge about clinical trials, data management, pharmacovigilance, regulatory issues and other major aspects of pharmacovigilance.
The program objective is to understand the key concepts in the responsible conduct of research and that conforms to the highest standards for the protection of human research subjects. It can be able to critically appraise the medical scientific literature, including the methodology of published and proposed investigations. It can be able to independently formulate a research question, as well as be able to design and conduct a study to address that question. It can be able to present and publish the results of one’s scholarly work. It is to identify a focus for future research and scholarly work, and to develop special expertise in the corresponding clinical domain and/or research methods. It would help you to gain in-depth knowledge on the best way to collect and report adverse events and safety data and manage the risk associated with and risk to your products. This advanced training pharmacovigilance short courses in India provide you with the unique format skills and knowledge that needed to operate a fast, effective drug safety or pharmacovigilance program. We provide best diploma, graduate and post graduate certificate courses to college students to enhance their start up in clinical research and pharmacovigilance.
*Fees subject to taxes & exchange rates.
*Fees subject to taxes & exchange rates.
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Clinical research involves conducting studies to evaluate the safety and efficacy of new medical treatments, drugs, or devices in human subjects. Pharmacovigilance, on the other hand, focuses on the detection, assessment, understanding, and prevention of adverse effects or any other drug-related problems.
Yes! With the increasing emphasis on drug safety and regulatory compliance, there is a growing demand for professionals in pharmacovigilance.
Individuals with a background in life sciences, pharmacy, medicine, nursing, or related fields are eligible for pharmacovigilance courses.
Pharmacovigilance and medical coding are different fields with distinct roles. Pharmacovigilance focuses on drug safety and adverse event reporting, while medical coding involves assigning codes to medical diagnoses and procedures for billing and record-keeping. The choice depends on individual interests, skills, and career goals.
Yes, due to increased regulatory scrutiny and the need for pharmaceutical companies to ensure the safety of their products, pharmacovigilance is in demand.





















































