Taking a medicinal product through clinical development is already a long, complicated and expensive exercise, but developing an ATMP is likely to be more complicated, more expensive and presents particular challenges and opportunities for pharmacovigilance and drug safety.
TORONTO (PRWEB)
September 29, 2021
Advanced therapy medicinal products (ATMPs) are medicines for human use that are based on genes, tissues or cells. Taking a medicinal product through clinical development is already a long, complicated and expensive exercise, but developing an ATMP is likely to be more complicated, more expensive and presents particular challenges and opportunities for pharmacovigilance and drug safety.
These challenges often take the form of:
-
Idiosyncratic protocol design - Proactive detection of risks
- Risk mitigation and treatment frameworks
- Long-term follow-up obligations
Register for this webinar to explore those challenges and the means to address those opportunities to add real value in the management of ATMP clinical trials.
Join experts from Arriello, Kieran O’Donnell, Principal Consultant, Pharmacovigilance; and Esther Poole, Managing Consultant, Clinical Safety, for the live webinar on Thursday, October 14, 2021 at 11am EDT (4pm BST/UK).
For more information, or to register for this event, visit Advanced Therapy Medicinal Products (ATMPs) in Clinical Trial Safety Services.
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