Half Introduction to Regulatory Affairs Course
Price
£689.00 Sale Price
Duration
4 Weeks
About the Course
Early booking discount ends in August
Introduction to Regulatory Affairs Course
Are you looking for an entry level role in regulatory affairs?
Gain work experience in regulatory affairs even if you are new to this field.
Enrol in the most comprehensive regulatory affairs introductory course available, which includes expert help with your CV and interview preparation (Full Course).
If you are interested in becoming a regulatory affairs professional but have no experience, or if you are working as a regulatory affairs professional but would like to have a strong foundation on the basics of regulatory affairs, then this course is suitable for you.
The Half Introduction to Regulatory Affairs Course Includes:
10+ CPD Hours of Regulatory Lectures covering the full medicines lifecycle
Case Studies
EU, UK and US Regulations
Certificate
On Demand Recordings for your to learn at your own pace.
Available from September 2024
View the course brochure for full information
Klarna can be used to purchase this product: Pay in 30 days or Pay in 3 installments.
If you are having any technical difficulties paying for the course, then please email contact@entrytoregulatory.com to request an invoice.
Discounted prices may be available for those who are in full time education, those working for charities full time, those from low income countries and those working in academia or goverment agencies. contact contact@entrytoregulatory.com to enquire.
Discounts are available for multiple bookings. Moreover, in-house training is available. Please contact contact@entrytoregulatory.com to enquire.
Returns Policy: A 14-day cooling off period applies. If you change your mind during this period before accessing the course, you will receive a refund less a cancellation charge of £50 for normal transactions or £100 if Klarna was used. If you access the digital content in any way, your right to refund is waived. No refund will be given if you have viewed any of the content purchased. The registration is non-transferrable.
Your Instructor
Rabiea
Rabiea, Principal Regulatory Consultant and Managing Director
I am a UK registered pharmacist with around ten years of regulatory affairs experience gained from working in the UK regulatory health authority (MHRA) as an Assessor and several global pharmaceutical companies companies, such as, GSK, MSD and Bayer.
My experience covers the entire product lifecycle, from clinical trial applications through to new drug applications and post-approval changes. I have worked on various different medicinal products, including biologicals, vaccines, medical device combinations, consumer products (OTC), small molecule and generic medicinal products.
I have successfully delivered multimillion-dollar regulatory approvals and cost savings repeatedly for several pharmaceutical companies throughout the EU, US, UK, and the rest of world markets.
I am passionate about regulatory affairs and providing exceptional regulatory support for pharmaceutical companies to accelerate innovation and deliver for patients. Furthermore, I am passionate about training other regulatory professionals in complex regulatory topics.