Complete Pharmacovigilance Training Certificate Course-2025
What you'll learn
- Introduction to Pharmacovigilance
- Overview of Pharmacovigilance course
- Basics of Pharmacovigilance
- Career oportunities in pharmacovigilance
- Terminologies in PV
- History of PV
- Drug Discovery and Development
- Job roles in PV
Requirements
- Pharmacy background of any lifesciences graduation/post graduation
- Medical background
- Curiosity towards learning skills
Description
Pharmacovigilance, which is one of the unique careers, is associated with life science and pharmacy. The role of this scientific discipline is to analyse the side effects of drugs; they monitor the safety of drugs that are available in the market. Whenever any effect is reported, the pharmacovigilance professionals are the ones who follow up with the case and carry out the necessary tests, etc. accordingly.
What is Pharmacovigilance (PV)?
Pharmacovigilance monitors the safety of a drug once it has been launched onto the market. It is the process which improves the safety of medicines. It detects medicines that cause serious adverse drug reactions (ADRs) and ensures they are re-evaluated or removed from the market to protect public health.
As such, pharmacovigilance heavily focuses on adverse drug reactions (ADR), which are defined as any response to a drug which is noxious and unintended, including lack of efficacy (the condition that this definition only applies with the doses normally used for the prophylaxis, diagnosis or therapy of disease, or for the modification of physiological disorder function was excluded with the latest amendment of the applicable legislation).
Pharmacovigilance, which is one of the unique careers, is associated with life science and pharmacy. The role of this scientific discipline is to analyse the side effects of drugs; they monitor the safety of drugs that are available in the market. Whenever any effect is reported, the pharmacovigilance professionals are the ones who follow up with the case and carry out the necessary tests, etc. accordingly
Career Opportunities in PV:
Pharmacovigilance job profiles are Pharmacovigilance Associate, Drug Safety Associate, Clinical Data Manager, Senior Drug Safety Associate, Pharmacovigilance Scientist, Clinical SAS Programmer, etc. A pharmacovigilance professional earns INR 2,00,000 - 8,00,000 per annum on average. According to Glassdoor, the national average salary of a Pharmacovigilance professional is INR 3,01,464 per annum.
Pharmacovigilance jobs for freshers pay INR 1,90,000 - 2,50,000 per annum. After 2 -3 years of experience, pharmacovigilance salary is INR 4,80,000 - 10,00,000 per annum. A freelancer in Pharmacovigilance can earn an average of INR 1,00,000 - 8,00,000 per annum.
TCS, IQVAI, Cognizant, Wipro, Accenture are top pharmacovigilance companies and pay the highest pharmacovigilance salary of INR 4 - 9 lakhs per annum.
Pharmacovigilance Scope:
India is one of the largest producers of pharmaceuticals in the world and is popular even for exporting the pharmaceuticals. There are more than 8000 licensed drug manufacturers in India which will recruit pharmacovigilance professionals in good numbers. There are many job opportunities abroad, in countries like the United States and the European countries, too.
Pharmacovigilance also known as PV are activities that are related to the detection, assessment, understanding and prevention of adverse long term as well as short term side effects of medicine.
There are two important duties i.e. analyzing and identification of hazards of various medicines and preventing patients from wrong medications.
In short, it is the duty of pharmacovigilance professionals to collect adverse data on the companies’ products, analyze the data, recommend the changes and warnings in labelling or clinical trial protocols.
To become a pharmacovigilance professional a degree in Life Science is required. They must have the knowledge of medical terminology, pharmaceuticals or nursing.
One must have information management skills, communication and foreign language skills, ethical, legal and regulatory knowledge to be successful in the field.
India is the fourth largest producer of pharmaceuticals in the world and has more than 8,000 licensed drug manufacturers along with 60,000 branded formulations that will create various job opportunities for Pharmacovigilance professionals.
Accenture, Cognizant, IQVAI Limited, TCS, Novartis, APCER Life Sciences, etc are some of the top paying companies.
Eligibility for course:
Candidates who have graduated from life sciences degree such as botany, zoology, biotechnology, microbiology, biochemistry, genetics, etc. are eligible to pursue this field.
Any Lifescience Graduates/Post graduates
Pharmacy background
Bachelors of Pharmacy
Masters in Pharmacy
MBBS doctors/Physician
Nurses
Dentists
Goals of This course:
To know thorough knowledge on PV
To know concepts in PV
To know the basic terminologies in PV
To become familiar with PV profession
What is Drug Discovery and development
To know role of PV Professional in Pharma industry
To become skilled PV professional
To learn PV
To take Certification of course
Benefits of PV course:
Add on skill in professional profile
New job opportunities in PV
Certification of completion
Self development
Continuous learning
Update in knowledge
Practice Quiz
Improvement is a continual process.
"Be it products, services or human beings we tend to improvise with innovation and always change and grow over time. Being stagnant or stuck with oneself will not make you successful."
Who this course is for:
- Pharmacy background of any lifesciences graduation/post graduation
- Freshers looking for Pharmacovigilance jobs n India/US/Canada
- Anyone can apply who are seeking job opportunities in Pharmacovigilance
- Bachelors of pharmacy
- Masters of Pharmacy
- Diploma/Graduates/Post graduates in Lifescience
Instructor
I Am Mahesh Pratapwar.
I am Pharma Professional, having skill of Pharmaceutical Product development and Complying with Regulatory Specifications for Pharmaceutical products according to guidelines of US/Europe/CDSCO.
I have completed M.Pharm (P.Ceutics).
Work experience more than 6 years in Pharma Industry.
Regulatory Affairs plays a crucial role in the pharmaceutical industry and is involved in all stages of drug development and also after drug approval and marketing. ... Pharmaceutical companies use all the data accumulated during discovery and development stages in order to register the drug and thus market the drug.
Skills: Formulation & Development, Stability studies, QbD, OSD, Oral Liquids, Topical/Derma, DRA, CTD & eCTD, Plant exposure, Bioequivalence, DoE, etc...
Published more than 3 Research and review articles in high impact journals.
Top 9 pharma courses has been published on Udemy
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5. Complete Qbd: Quality by Design in Pharmaceutical Product Development
6. DOE-Design of Experiment in pharmaceutical development
7. Regulatory Affairs USFDA Electronic Submission Course
8. GMP Tablet Manufacturing Technology & Pharmaceutical Practices.
9. IPQC tests for Pharmaceutical Tablet dosage form
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