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Free Regulatory Affairs Course Do you want to learn about regulatory affairs? If so, register for this free course. (Join link at the bottom of the page⬇️) This is a 3 hour self-paced recorded course that you can do in your own time. There is even a work experience assignment and case study for you to try out. ❌ The answers to the work assignment are in the certified course So if you are interested in investing in yourself and starting your professional journey in regulatory affairs, join today. ❌ This course does not provide a certificate. Join the certified course for a certificate 📜 https://www.entrytoregulatory.com/challenge-page/regulatory-affairs-certificate-course?programId=6a2af3d8-1d3e-4c98-8968-30627cae6a4d What you will learn: - How to develop a regulatory strategy for a MAA - What is in a Marketing Authorisation Application? - What is in the CTD (overview)? - How to classify an EU variation? - How to author Module 1 of the CTD - QP declaration - What is the drug development process? - What is regulatory affairs? - Why have a career in regulatory affairs? - What salary do regulatory affairs professionals get? (and benefits) - Career progression in regulatory affairs - What do regulatory affairs professionals do? - How to get a job in regulatory affairs? - Information about the full Introduction to Regulatory Affairs Course - How to get regulatory affairs work experience and job mentoring It is based on the content of the full Introduction to Regulatory Affairs course, which provides 40+ CPD hours of learning, real regulatory work experience / internship and job search support. So by doing this course, you get a sneak peak of the full regulatory course. Our expert course tutor has over 10 years of regulatory affairs experience in the UK regulatory health authority and large pharmaceutical companies such as GSK, MSD and Bayer. Don't forget to share the course link with your friends and colleagues
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