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Online Training in Regulatory Affairs | Online Regulatory Affairs Training Course | Pharmacovigilance
Online Training in Regulatory Affairs | Online Regulatory Affairs Training Course | Pharmacovigilance Online
Pharmacovigilance is a field of science that primarily deals with determining, verifying, quantifying, analyzing and reducing the ill effects of medical drugs, devices or biologicals, thus increasing their safety.
Pharmacovigilance is an anchor throughout the life cycle of new drugs and devices due to a demand created by the requirement of new medical treatments and their legislation.
With the global financial drift and the promise shown by emerging nations such as India, China, Brazil and Russia, the drug development industry is moving its R & D and pharmacovigilance activities towards these regions for better efficiency and cost savings.
At the core of clinical research and pharmacovigilance is the area of regulatory affairs. Regulatory Affairs teams are well aware about local and international regulations pertaining to research activities, marketing of drugs etc and help facilitate innovation and reducing the time to market of promising new therapies.
In today’s drug development landscape with fierce competition among pharmaceutical companies, people with formal training in regulatory affairs spearhead large global projects from a regulatory perspective and make sure that studies are carried out as per the applicable regulatory requirements.
At James Lind Institute we transform students interested in pharmacovigilance & regulatory affairs into seasoned professionals up-to-date with the most recent knowledge and trends. The Advanced PG Diploma in Pharmacovigilance and Regulatory Affairs course is practically driven and structured on the responsibilities expected of a pharmacovigilance & a regulatory affairs professional in the drug development industry. Candidates enrolled in this highly focused pharmacovigilance and regulatory affairs program are equipped with the knowledge of the global regulatory landscape and acquire skills necessary for regulatory strategic planning throughout the product life cycle.
Self Paced 6 - 8 months (Maximum duration 24 months)
A student for the Advanced Post Graduate Diploma in Pharmacovigilance & Regulatory Affairs (APGDP-RA) is expected to study online for a minimum of fifteen hours per week.
Course assessment involves online multiple choice questions for each lecture, followed by assignments for each study module.
The minimum eligibility criteria for the course would include either of the following:
MBBS/BHMS/BAMS/BPT/MPT/BDS/BMLT/Bachelor in Naturopathy & Veterinary Science /MD/MS.
Graduate/Postgraduate degree in Pharmacy/ Pharmaceutical Sciences.
Graduate/Postgraduate degree in Life Sciences (Botany, Zoology, Biochemistry, Microbiology, Genetics, Biotechnology).
Graduate/Postgraduate degree in Chemistry/Biostatistics/ Bioinformatics.
Graduate or equivalent degree in Nursing/Allied Health.
Students in their final year of graduation for the above courses may also apply.
Course fee for all JLI courses is very reasonable. Please use our Course Fee Calculator below to know the course fee applicable to you.
If you are not sure about the fee applicable to you for Advanced Post-Graduate Diploma in Pharmacovigilance and Regulatory Affairs, please send an email to firstname.lastname@example.org or chat with our online counsellor.
For more details about the admission procedure please click here.
Throughout the course, the students can interact with the faculty and other students via the “Online Campus Tutoring Centre” to discuss any coursework related issues.
Each student in the Advanced Post-Graduate Diploma in Pharmacovigilance and Regulatory Affairs course is assigned a mentor throughout the course who is a senior professional from the Industry. Students are in close contact with the “Student Success Team” during the course and thereafter as alumni. To know more about the “Student Success Team”, click here.