When: 30 July - 1 August 2025
Where: TOPRA Office, 3rd Floor, City Reach, 5-6 Greenwich View Place, London, E14 9NN
Day 1 start time: TBC | Day 3 end time: TBC
This course is also available to attend online.
Suitable for
This course is essential for:
- Delegates from the pharmaceutical industry who wish to develop their knowledge
- Delegates from allied industries who wish to have a comprehensive understanding of the subject
- Students on the TOPRA MSc programme.
Note: this course is also Module 24 of the MSc Regulatory Affairs.
Course information
The aims of this course are to enable delegates to consider and evaluate practical regulatory aspects of regulatory affairs in the Middle East and North Africa (MENA). Delegates will also explore and critically debate the regulatory issues likely to arise during drug development to be able to provide effective advice on the regulatory affairs activities involved with drug development in the MENA region.
Benefits for delegates
This course will enable you to:
- Possess a systematic understanding of knowledge, and a critical awareness of the regulatory environment and procedures governing regulatory approval of clinical trials in the MENA region and regulatory marketing authorisation in the context of drug development.
- Demonstrate a conceptual understanding of the regulatory requirements, regulatory bodies requirements, regulatory authorisation and associated documentation for marketing submissions.
- Demonstrate originality in the application of knowledge of the MENA region regulatory aspects of drug development to evaluate critically current research in the discipline.
CPD: This course provides 19 CPD hours upon successful completion.
To learn more about why Continuing Professional Development is important, visit our Lifelong Learning page.
Programme
Further details will be released in the near future.
Module Leader
 |
Farida Alayan, Intellectual Property & Regulatory Affairs Consultant, Trainer, and
Expert in Pharmaceutical IP, RA & Data Exclusivity, MENA & UK |
Presenters
Further details will be released in the near future.
Pricing
| Standard training course registration fees |
| Event Registration Type |
Price (GBP) |
Standard Price
TOPRA Member |
£1,900.00 + VAT* |
Standard Price
Non-member |
£2,375.00 + VAT* |
TOPRA MSc Students
|
£1,650.00 + VAT* |
Save on the full cost of membership and £180 on the price of your training
course when you add TOPRA membership to your booking (membership fees are exempt from VAT).
*VAT, where applicable, is charged at the rate of 20%.
| Discounted training course registration fees |
| Event Registration Type |
Price (GBP) |
Government or academic rates
TOPRA Member
|
£1,425.00 + VAT* |
Government or academic rates
Non-member
|
£1,781.25 + VAT* |
Charities, patient groups, full-time education rates
TOPRA Member |
£950.00 + VAT* |
Charities, patient groups, full-time education rates
Non-member
|
£1,187.50 + VAT* |
Places are also available for those in low-income countries as defined by the World Bank.
*VAT, where applicable, is charged at the rate of 20%.
Please email meetings@topra.org for a discount code before making your booking.
Terms and conditions
By booking a place on this course you are agreeing to the training terms and conditions.