We provide online one-on-one counselling and Q&A sessions to ensure online learning is beneficial for the aspirants. Our mentors help aspirants clear their doubts and queries and get all the answers they need.
Missed a live lecture? Don\u2019t worry. You can always find a recorded lecture on our platform and revisit it as many times as you want during the course duration.
Getting the course once will help you prepare for not one but multiple attempts. You get access to all the resources for more than a year, to ensure proper revision.
We help you get in touch with a community of experts, which includes mentors, registered practitioners, previous alumni and those who have successfully cleared the exams. This adds value to your preparation and get all the guidance and motivation you need.
Yes. The PGCert is designed for part-time learners and physician schedules. Many graduates balance clinical practice with PV work or move into hybrid roles.
The PGCert prepares you for medical reviewer and safety physician roles. Senior leadership roles typically also require multi-year PV experience. The certificate accelerates entry and early progression.
Yes. Coding accuracy is a programme staple with practical exercises and tools clinicians will use in real roles.
Common hirers are:
. Large pharma
. Biotech
. CROs
. Regulators
. Hospitals
. Specialist consultancies
Graduates can work as
· Drug Safety Physicians
· Medical Reviewers
· Safety Scientists
· Pharmacovigilance Leads
Absolutely. Pharmacovigilance offers stable, global, and high-impact careers. Doctors use their clinical expertise to ensure medicine safety worldwide.
No. The course starts from the fundamentals and gradually builds up to advanced safety and regulatory topics. It is ideal for clinicians new to industry roles.
Indeed, there is. We offer
· Career mentoring
· Resume guidance, and
· Interview preparation
All this to help graduates transition smoothly into PV roles.
A Drug Safety Physician (DSP), also called a Pharmacovigilance Physician, is a medical doctor who monitors and evaluates the safety of medicines once they are in clinical trials or on the market. Their job is to assess adverse drug reactions (ADRs) and ensure patient safety through evidence-based evaluation and reporting.
This role is primarily for medical graduates (MBBS, MD, or MS) and foreign medical graduates who wish to transition into the pharmaceutical or clinical research industry. Some Dental (BDS/MDS), AYUSH, PharmD, or PhD professionals with a strong clinical or pharmacology background are also eligible and are often considered by companies for Drug Safety and Pharmacovigilance roles.
It’s one of the best non-clinical careers for doctors who want to stay connected to clinical science without hospital work. You use your medical judgment to analyze drug safety data, help improve treatments, and earn competitive salaries, often ₹20–35 Lakh/year in global roles.
They review clinical trial and post-marketing safety reports, assess causality, write medical narratives, and collaborate with regulatory and pharmacovigilance teams to ensure drug safety compliance (per ICH-GCP, FDA, CDSCO and EMA standards).
Many companies accept foreign medical graduates (without FMGE) as well.
You’ll gain hands-on understanding of:
After certification, you can apply for roles like:
Medical Reviewer / Safety Scientist
These positions exist in pharma companies, CROs, and global pharmacovigilance organizations.
In India, entry-level Drug Safety Physicians typically earn ₹8–15 Lakh/year, while experienced professionals or those working with global CROs can earn ₹25–40 Lakh/year.
In the US, UK, or Australia, salaries range between USD $80,000–$140,000 per year.
Yes. It’s ideal for doctors who are waiting for exams, results, or residency, and want to build an industry-ready, non-clinical skillset. The knowledge of pharmacology and safety can also support future global healthcare roles.
You can progress from Drug Safety Associate → Medical Reviewer → Safety Physician → Global Safety Leader / Medical Director (Pharmacovigilance).
With experience, you can move into Medical Affairs, Regulatory Affairs, or Clinical Development.
Get proven tips from experts on building a robust resume to help you land your dream job.
Chisel your interview skills to ensure you mesmerise the interviewers into giving in.
Receive support at each step of your journey- during your exam preparation and beyond.
Yes. The PGCert is designed for part-time learners and physician schedules. Many graduates balance clinical practice with PV work or move into hybrid roles.
The PGCert prepares you for medical reviewer and safety physician roles. Senior leadership roles typically also require multi-year PV experience. The certificate accelerates entry and early progression.
Yes. Coding accuracy is a programme staple with practical exercises and tools clinicians will use in real roles.
Common hirers are:
. Large pharma
. Biotech
. CROs
. Regulators
. Hospitals
. Specialist consultancies
Graduates can work as
· Drug Safety Physicians
· Medical Reviewers
· Safety Scientists
· Pharmacovigilance Leads
Absolutely. Pharmacovigilance offers stable, global, and high-impact careers. Doctors use their clinical expertise to ensure medicine safety worldwide.
No. The course starts from the fundamentals and gradually builds up to advanced safety and regulatory topics. It is ideal for clinicians new to industry roles.
Indeed, there is. We offer
· Career mentoring
· Resume guidance, and
· Interview preparation
All this to help graduates transition smoothly into PV roles.
A Drug Safety Physician (DSP), also called a Pharmacovigilance Physician, is a medical doctor who monitors and evaluates the safety of medicines once they are in clinical trials or on the market. Their job is to assess adverse drug reactions (ADRs) and ensure patient safety through evidence-based evaluation and reporting.
This role is primarily for medical graduates (MBBS, MD, or MS) and foreign medical graduates who wish to transition into the pharmaceutical or clinical research industry. Some Dental (BDS/MDS), AYUSH, PharmD, or PhD professionals with a strong clinical or pharmacology background are also eligible and are often considered by companies for Drug Safety and Pharmacovigilance roles.
It’s one of the best non-clinical careers for doctors who want to stay connected to clinical science without hospital work. You use your medical judgment to analyze drug safety data, help improve treatments, and earn competitive salaries, often ₹20–35 Lakh/year in global roles.
They review clinical trial and post-marketing safety reports, assess causality, write medical narratives, and collaborate with regulatory and pharmacovigilance teams to ensure drug safety compliance (per ICH-GCP, FDA, CDSCO and EMA standards).
Many companies accept foreign medical graduates (without FMGE) as well.
You’ll gain hands-on understanding of:
After certification, you can apply for roles like:
Medical Reviewer / Safety Scientist
These positions exist in pharma companies, CROs, and global pharmacovigilance organizations.
In India, entry-level Drug Safety Physicians typically earn ₹8–15 Lakh/year, while experienced professionals or those working with global CROs can earn ₹25–40 Lakh/year.
In the US, UK, or Australia, salaries range between USD $80,000–$140,000 per year.
Yes. It’s ideal for doctors who are waiting for exams, results, or residency, and want to build an industry-ready, non-clinical skillset. The knowledge of pharmacology and safety can also support future global healthcare roles.
You can progress from Drug Safety Associate → Medical Reviewer → Safety Physician → Global Safety Leader / Medical Director (Pharmacovigilance).
With experience, you can move into Medical Affairs, Regulatory Affairs, or Clinical Development.