When: 19 September 2019
Where: Lincoln Plaza London, 2 Lincoln Plaza, Canary Wharf, London E14 9BD
Time: 09.00 - 17.00
Course overview
Find the balance in providing just the right amount of information to assure your dossier fits with your regulatory strategy and on-going compliance needs. This course will help you understand the critical attribute of QBD and CQA in pharmaceutical development, and the importance of development pharmaceutics in helping the pharmaceutical assessor, whilst minimising future life-cycle maintenance of the MAA dossier.
Benefits to delegates
- Learn by doing - Participate in case studies and interactive sessions
- Build a network to support the rest of your career
- Meet and learn from experts in the field
- Take a course developed by professionals, for professionals - with a proven track record
CPD: This course provides 8 CPD hours upon successful completion
To learn more about why Continuing Professional Development is important, visit our Lifelong Learning page.
Programme
The latest course programme can be downloaded here.
Suitable for
Those who are responsible for reviewing dossiers for managers or for outsourced work and those involved in due diligence
Pricing
Course *fees:
| Type |
Member |
Non-member |
| Standard |
£550+VAT |
£675+VAT |
Discounted places
A limited number of discounted places are available at the rates below.
Please email us at meetings@topra.org for a discount code before making your booking.
|
|
Those working for regulatory agencies, government agencies or academic institutions
|
£412.50+VAT
|
£506.25+VAT |
Those working for charities, patient groups or in full-time education
|
£275+VAT |
£337.50+VAT |
|
*VAT, if applicable, is charged at the rate of 20%
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