Presented by
Management Forum
Global Pharmaceutical Regulatory Affairs Summer School In-house Training
Embark on Global Pharmaceutical Regulatory Excellence: Master Pharmaceutical Compliance Worldwide with Our Comprehensive Pharmaceutical Regulatory Affairs Course.
Unlock the world of pharmaceutical regulatory excellence with our Global Pharmaceutical Regulatory Affairs training – an intensive journey through the diverse regions, offering practical insights, expert guidance, and strategic mastery for professionals seeking to navigate and succeed in the dynamic global regulatory landscape.
- Format: Bespoke training
- CPD: 84 hours for your records (depending on your requirements)
- Certificate of completion
- Pharmaceutical Regulatory Affairs in Africa
- Pharmaceutical Regulatory Affairs in Asia
- Pharmaceutical Regulatory Affairs in China
- Pharmaceutical Regulatory Affairs in Latin America
- Pharmaceutical Regulatory Affairs in the Middle East
- Pharmaceutical Regulatory Affairs in Russia and the Eurasian Union
- The Common Technical Document (CTD) Submission in the MENA Region
- US FDA - Understanding Key Factors When Working with the FDA
- Global Pharmaceutical Regulatory Affairs Summer School
Overview
Navigate the ever-changing landscape of pharmaceutical regulations worldwide and ensure compliance by attending our Global Pharmaceutical Regulatory Affairs course – an indispensable resource for professionals seeking to stay current, mitigate risks, and thrive in the dynamic global pharmaceutical environment.
In an industry defined by evolving complexities, staying ahead is not just an advantage, but a necessity. This intensive summer school ensures a 360-degree understanding of global regulatory dynamics and has been designed to allow comprehensive exploration of regulatory landscapes in key regions.
Our expert-led courses provide practical insights, interactive case studies, and strategic guidance, equipping you with the knowledge to navigate diverse regulatory environments. Participants will not only grasp theoretical concepts but also hone the skills required to implement them in real-world scenarios.
This Summer School is made up of the following modules, the EU, Asia, Africa, Latin America, Russia & the Eurasian Union, the Middle East, and China. You can attend the entire Summer School, or mix and match modules to best suit your professional needs.
Please contact us for pricing of bespoke modules, info@ipi.academy.
This course is part of our Regulatory Affairs Training course collection, which features updates on the latest regulations to registration procedures and strategies.
Benefits of attending
- Gain a holistic understanding of regulatory affairs across diverse global regions.
- Acquire practical insights through case studies and discussion.
- Receive expert guidance from seasoned trainers with regional expertise.
- Learn to develop regulatory strategies for product approval in diverse markets.
- Understand regulatory reforms and updates.
- Explore regulatory authorities and requirements.
Who should attend?
- Pharmaceutical Regulatory Affairs Personnel
- Project Managers
- Clinical Development Professionals
- Business Planners
- Commercial Management Professionals
- Manufacturing Professionals
- Technical Staff
- Quality Assurance/Quality Control
This seminar will be of particular interest to all those who need to learn about successful marketing authorisation applications and in-market regulatory compliance in various regions around the world. You will find this seminar useful both as an introductory or refresher course.
