What are the courses in pharmacovigilance?
Courses on Pharmacovigilance
| Course Type | Conducted by Institute | Course Duration |
|---|---|---|
| Certificate Course in Pharmacovigilance | Symogen (KPO) | 4 Months |
| Post-graduate Diploma programme in Pharmacovigilance | Institute of Clinical Research | 1 Year |
What is the qualification for pharmacovigilance?
The basic qualifications for a career in pharmacovigilance include undergraduate or graduate degree in pharmacy, human or veterinary medicine, nursing, biochemistry, biotechnology, microbiology or allied health sciences.
Who can work in Pharmacovigilance?
In order to pursue a career in pharmacovigilance, the minimum eligibility criteria to apply for the course is: A postgraduate or graduate degree in Bioscience/Life Sciences (with any of the following subjects: Botany, Zoology, Biochemistry, Microbiology, Genetics, Biotech) with at least 50\% marks in aggregate.
What is the process of Pharmacovigilance?
Pharmacovigilance process Detection: Collection of Individual Case Safety Reports (ICSRs) Assessment Understanding and Prevention of adverse effects
What is the scope of pharmacovigilance in it?
Pharmacovigilance is also known as drug safety and it focuses on ADR (Adverse drug reaction).The main aim of Pharmacovigilance is to monitor approved drugs and Investigational new drugs for Ultimately PV is all about minimizing the risk to the patient by collecting and assessing data for products in the market and products under clinical trial
What are pharmacovigilance services?
Pharmacovigilance Services. There is an advantage in centralizing all safety data, clinical data, analysis and reporting with one provider. By combining Quanticate’s substantial biometrics, medical writing, and pharmacovigilance expertise, we offer a fully compliant and high-quality complete package of pharmacovigilance services.
What is pharmacovigilance system master file?
The pharmacovigilance system master file is actually a detailed description of the pharmacovigilance and safety procedures which a company follows when handling a product. It is a very useful document for the regulators and the MAH which ensures that noncompliance issues or deficiencies in the pharmacovigilance system will get detected.