Archives: Resources
Outsourcing lifecycle maintenance to a dedicated FSP regulatory affairs partner
Ensure adherence to regulations and the continuous supply of drugs to target markets
Ensuring effective regulatory intelligence in pharmacovigilance
Discover key pharmacovigilance regulatory intelligence capabilities for accuracy and cost-effectiveness
Long-term follow-up considerations for cell and gene therapies
Experts share insights when considering long-term follow-up studies in the CGT space
The 2024 FSP trends webinar
Experts discuss the future of FSP strategies and models
Establishing a bespoke outsourcing arrangement with hybrid FSP/FSO partnerships
Optimizing your clinical trial operations with a hybrid FSP/FSO model
Unique considerations in pediatric clinical research
Explore the intricate challenges of pediatric clinical research with our rare disease and pediatric experts.
The 2024 sites and patients trends report
Explore challenges, sentiments and keys to success facing research sites and patient recruitment efforts in this new report.
Cracking the talent shortfall: strategies for delivering the right talent with an FSP model
FSP Models deliver the right talent. Explore expert strategies in this CenterWatch article.
Optimizing the cell and gene therapy patient journey through integrated CRO/CDMO partnership
Optimizing the patient journey starts with a unified approach to clinical development. Read more.