Where: TOPRA, 6th Floor, 3 Harbour Exchange, South Quay, London, E14 9GE, United Kingdom
When: 7 December 2017
View the programme
This course is ideal for:
-
Experienced staff from related disciplines, e.g. manufacturing, marketing and sales
-
Support staff
-
Anyone requiring an overview of regulatory affairs
What previous delegates have had to say about this course
“ Speakers very clear, concise and informative” |
|
|
|
|
“ Excellent overview in such a short time!” |
“ Well structured set of presentations and very informative.” |
|
|
|
|
“ Made things a lot clearer and gave me an understanding of how things link together.” |
What you will learn
-
Background to regulatory affairs
-
The European legislative framework
-
Overview of drug development
-
Overview of clinical trials
-
Marketing Authorisation Applications
-
Labels and leaflets
-
European Procedures
-
Lifecycle management, including variations
-
This course will give a basic grounding in a relaxed, enjoyable environment.
CPD
This course offers 5 CPD hours for successful completion, to learn about why CPD is important visit the Lifelong Learning page.
This course is now full, to be added to the waiting list, please email meetings@topra.org.
Please read the training terms and conditions before booking this course. By booking a place on this course you are agreeing to the training terms and conditions.
Course prices:
Registration Fee: £580+VAT
Discounts:
Discounts are offered to groups listed below. Please ensure you email us for the discount code before making your booking.
Those working for regulatory agencies or government agencies or academic institutions:
Registration Fee: £435+VAT
Those working for charities, patient groups or in full time education:
Registration Fee: £290+VAT
- Please note the number of discounted places may be limited.
- All fees are shown in Pounds Sterling and do not include VAT
- Fee excludes accommodation and travel. The delegate ticket includes refreshments at coffee breaks and buffet lunches (if applicable)