Date :
Early development activities can be complex and this interactive half-day session will help you to understand the do’s and don’ts when planning your CTA/IND programme. Our team of regulatory professionals will focus on aligning development and regulatory activities and the importance of integrated development plans, helping achieve accelerated development in Europe and the US.
Agenda
1.00 Registration, refreshments and networking
1.30 Introduction to Boyds
1.45 Nonclinical development programmes to support first in-human studies
2.30 Preparing clinical trial applications for Europe and the US
3.30 Refreshments and networking
3.45 Using clinical data to maximise regulatory value
4.45 Close
To reserve your place, please register by 11 March 2020 - email [email protected] or ring 01270 270010 to register.
Cost: £175 +VAT
Venue and Location Information:
The Cambridge Building at Babraham Research Campus, Cambridge, CB22 3AT
Event Registration Link: