Pharmaceutical Regulatory Affairs (Basic)

Course Details

The Pharmaceutical Regulatory Affairs (Basic) Course provides foundational knowledge on regulatory guidelines, compliance, and industry standards essential for pharmaceutical professionals.

Course starts

The course begins in the first week of April, providing structured learning and hands-on experience.

Course Fee

The course fee is INR 50,000, with an early bird offer of INR 30,000 for the first batch.

Duration of the course

A 10-week course with a commitment of 10 hours per week, designed for in-depth learning and skill development.

Compliance is the backbone of trust in healthcare. Begin your journey into regulatory excellence with us

1 : 1 Mock interview Assistance

Personalized one-on-one mock interviews for regulatory pharmacist roles, focusing on industry regulations, compliance, and expert feedback to enhance your interview success.

Expert-led training designed to provide industry insights, practical knowledge, and career-enhancing skills from seasoned professionals.

A tailored resume-building session to craft a professional, ATS-friendly resume that highlights your skills, experience, and strengths for better job opportunities.

Training from Industry Experts

Resume Building Session

Mr. Rizwan
A Seasoned Regulatory Affairs Expert

Meet Our Mentor

Extensive experience of over 15 years in pharmaceutical regulatory affairs, which includes leadership experience of 5 years and regulatory program and project management experience of 8+ years

• Mr. Rizwan is a highly proficient qualified in the industry.

• A pharmaceutical chemistry post-graduate turned regulatory expert, he currently contributes his expertise at Novo Nordisk in Copenhagen, Denmark.

• Throughout his career, he has held key roles at leading pharmaceutical companies such as Pfizer, Mylan, and Cipla.

• Originally from India, Mr. Rizwan has successfully navigated an inspiring career path, transitioning to Europe and making significant contributions to global regulatory affairs.

• His expertise spans diverse regulatory verticals, including CMC, medical devices, and international regulatory submissions across the US, EU, and other global markets.

• He is also deeply engaged in interpreting evolving regulations and spearheading advocacy initiatives.

• Beyond his professional achievements, Mr. Rizwan is passionate about mentorship and has trained numerous colleagues, equipping them with the knowledge and skills to excel in regulatory affairs.