Date: 5 September 2019
Time: 12:00 - 13:00 BST (GMT+1)
Attendance for this event has reached capacity. Registration is now closed.
This webinar will cover the nonclinical requirements in bringing biotechnology-derived therapeutics to market and will include a broad and basic understanding of the practical and legislative requirements for the nonclinical phase of drug development.
Case studies of nonclinical development of selected biotech products will be included as examples.
Speakers
Agenda
- Introduction – 5 mins
- Legal basis (EU Regulatory and legal framework) – 15 mins
- Nonclinical development plan – 15 mins
- Case reviews – 15 mins
- Q&A – 10 mins