Why should you attend
Attend this course if you would like to learn about ATMP development and regulation, you would like a forum to hear from experts in the ATMP field, or you are looking for an opportunity to discuss the challenges you have and share your experiences with others.
What will this course cover?
This course will cover an introduction to ATMPs, CMC and quality considerations for ATMPs, Non clinical development of ATMPs, experience in clinical development of ATMPs, Environmental risk assessments for GMOs in clinical trials, regulatory challenges and pitfalls.
The programme includes:
- Introduction to ATMPs
- CMC and Quality considerations for ATMPs – Part 1
- CMC and Quality considerations for ATMPs – Part 2 Food for Thought (examples of ATMP challenges).
- Non clinical development of ATMPs
- Experience in Clinical Development of ATMPs
- Environmental Risk Assessments for GMOs in Clinical Trials
- Regulatory Challenges and Pitfalls
CPD
This course offers 6 CPD hours for successful completion, to learn about why CPD is important visit the Lifelong Learning page.
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 price (to register, please log in or create an account):
Member: |
£550+VAT |
|
Non-member: |
£675+VAT |
Those working for regulatory agencies or government agencies or academic institutions:
Member: |
£412.50+VAT |
|
Non Member: |
£506.25+VAT |
Those working for charities, patient groups or in full time education:
Member: |
£275+VAT |
|
Non Member: |
£337.50+VAT |
For a discount please contact the professional development team for the code (please note the number of discounted places may be limited.)
- Fee excludes accommodation and travel. The delegate ticket includes refreshments at coffee breaks and buffet lunches (if applicable).