Basic course of 4 hours free
Completion certificate
AI tutor
Practical activities
Online and lifelong course
What will I learn?
Get a solid understanding of pharmaceutical regulatory affairs with this course wey dem design specially for pharmacy people. You go learn di important regulatory laws and how dem take dey work, including ICH, EMA, and FDA guidelines. You go become expert for preparing regulatory documents, from clinical trial data to label and manufacturing rules. You go learn all di inside and outside of how to submit documents, including how to prepare document and use electronic systems. You go get strategic compliance skills with quality control, risk management, and how to communicate well with regulatory authorities. Register now to make your career better.
Live mentoring sessions weekly
Rely on our team of specialists to assist you weekly
Imagine learning while clarifying doubts with those already in the field? At Apoia, this is possible
Gain access to open sessions with various market professionals
Expand your network
Exchange experiences with specialists from different areas and solve your professional challenges.
Learning outcomes
Enhance the development of the practical skills below
Know di regulatory laws well-well: Understand ICH, EMA, and FDA guidelines like di back of your hand.
Plan how to submit documents: Make correct timelines and find di important things wey you need to do.
Prepare regulatory documents: Make sure everything dey correct for clinical trials and labeling.
Use electronic systems well: Submit documents faster with new digital tools.
Put compliance strategies in place: Improve quality control and manage risk well.