When: 19 September 2019
Where: TOPRA. 6th Floor, 3 Harbour Exchange, South Quay, London, E14 9GE
Time: 09.00 - 17.00
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
CPD: This course provides 8 CPD hours upon successful completion
- 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
To learn more about why Continuing Professional Development is important, visit our Lifelong Learning page.
Those who are responsible for reviewing dossiers for managers or for outsourced work and those involved in due diligence
Book now at 2018 registration fees!
*VAT, if applicable, is charged at the rate of 20%
A limited number of discounted places are available at the rates below.
Please email us at firstname.lastname@example.org for a discount code before making your booking.
|Those working for regulatory agencies, government agencies or academic institutions
|Those working for charities, patient groups or in full-time education