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Regulatory Affairs
Regulatory Affairs is a key part of the pharmaceutical and life science fields. It helps ensure that products follow global laws during development, approval, and sale. This job involves preparing and submitting documents to health regulatory bodies, such as the FDA or EMA, to demonstrate that products are safe, effective, and of high quality.
The goal is to help products get approval on time and follow all the rules. People in this role help connect companies with health agencies, explain laws, and manage paperwork and talks. Their job helps bring good, legal products to the market and keeps them approved in many countries.
Eligibility & Duration
Working professionals in the Pharmaceutical and Life Sciences industries
- Candidates with the following educational backgrounds:
- Bachelor’s or Master’s degrees in Life Sciences, including:
Biotechnology
Microbiology
Biochemistry
Chemistry
Molecular Biology
Genetics
B.Pharmacy / M.Pharmacy
B.Tech / M.Tech in Biotechnology or related disciplines
Course Duration
The pharmaceutical regulatory affairs course takes 1 Month to complete and works well for working professionals.
Assessment & Certification
After the course is done, an online test is required. A score of 70% or higher is needed to pass. Anyone who passes will get a certificate accepted worldwide from Pharma Connections.
The course can be taken by new learners and those with experience. It’s available from anywhere.
Start now to grow your skills in Regulatory Affairs.
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Pharma Connections, Established on February 14, 2019, A Product of Eduteq Connections Pvt Ltd (An ISO 9001:2015 certified company), is dedicated to providing training and upskilling opportunities for Life science Professionals.
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