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Certified Regulatory Affairs Course (6 hours) 📜 Want to get a certification in regulatory affairs that covers global pharmaceutical regulatory requirements and includes real regulatory authoring? If so, register for this certified regulatory affairs course (Join link at the bottom of the page ⬇️) 6 hours of regulatory learning which includes: ✅ Regulatory affairs lectures ✅ Quizzes ✅ Regulatory affairs work experience ✅ Case study ✅ Certificate Rabiea, our expert Associate Professor tutor has over 10 years' of regulatory experience working for the UK Regulatory Health Authority (MHRA) and large pharmaceutical companies such as GSK, MSD and Bayer. This is a self-paced online regulatory affairs course that you can do in your own time. So, if you are interested in investing in yourself and starting your professional journey in regulatory affairs, join today. What you will learn: ✔️ What regulatory affairs is, the role, salary, skills and companies hiring ✔️ Drug development - drug discovery, pre-clinical (Phase 1, 2 and 3), clinical trials, MAA, NDA, variations ✔️ How to get regulatory affairs work experience and job mentoring ✔️ The ICH and global health authorities ✔️ United States regulatory procedures - FDA, IND, NDA, ANDA, BLA ✔️ European regulatory procedures - EMA, National Authorities, CTA, MAA, generics, regulatory strategy. The MHRA ✔️ CTD structure and content - Module 1, 2, 3, 4 and 5. ✔️ ASMF and DMFs ✔️ Global regulatory strategy case study - EU, UK, US, Switzerland, Singapore, Australia, Ukraine, UAE and South Africa ✔️ Bonus - Regulatory authoring tasks ✔️ EU variations classification ✔️ EU MAA Module 1 authoring The course content is a sample of the Full Introduction to Regulatory Affairs course, which also provides: ✅ 40+ CPD hours of learning, ✅ Regulatory affairs work experience / internship ✅ Job search mentoring Don't forget to share the course link with your friends and colleagues
You can also join this program via the mobile app. Go to the app