Boyds is hosting a half-day workshop focusing on early drug development.
Early development activities can be complex and this interactive half-day session will help you 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.
Date: 16 July 2020
1.00pm Registration and refreshments
1.00pm Introduction to Boyds
1.15pm Nonclinical development programmes to support first-in-human studies
2.00pm Preparing clinical trial applications for Europe and the US
3.15pm Using clinical data to maximise regulatory value
The workshop will be delivered by experienced members of the Boyds team.
Email email@example.com or phone 01270 270010 to book your place.