Pharmaceutical Regulatory Affairs Course

CertificatePreview

Content always updated in your course.

Basic course of 4 hours free

Completion certificate

AI tutor

Practical activities

Online and lifelong course

What will I learn?

Learn di main-main tins about how medicine business take run according to law wit dis full course wey dem design for people wey sabi pharmacy work. Dig deep inside di important law rules wey dey guide di work, like ICH, EMA, and FDA guidelines. Get correct knowledge about how to arrange paper work for di law, from data wey dem collect during trial to how dem suppose label medicine and di rules for how dem suppose make am. Learn di correct way to submit paper work, how to prepare all di documents and how to use computer systems. Learn how to follow di law by checking quality, managing risk, and talking to di people wey dey in charge of di law. Register now to make your career better.

Live mentoring rooms weekly

Rely on our team of specialists to assist you weekly

Imagine learning something while clearing your doubts with people who are actively working in the field? At Apoia, this is possible

Gain access to open rooms with various market professionals


Expand your network


Exchange experiences with specialists from other fields and resolve your professional challenges.

Learning outcomes

Strengthen your development in the practical skills listed below

Know di law rules well-well: Waka through ICH, EMA, and FDA guidelines wit confidence.

Plan how to submit paper work: Make correct time-table and know di important steps.

Prepare paper work for di law: Make sure say you follow law for clinical trials and labeling.

Use computer systems: Submit paper work quick-quick wit new digital tools.

Follow law strategies: Improve how you check quality and manage risk.