Archives: Resources
Managing Complex Sample and IP Logistics in Support of Cell and Gene Therapies
Read more about managing complex logistics around the escalating demands and scalability of CGT trials.
Strategic use of FSP models to expand trials into non-footprint countries
Read more about how to leverage FSP models to enhance global clinical trial reach and inclusion in the latest Contract Pharma.
Integrated CRO and CDMO Solutions
Integrated CRO and CDMO solutions encompass contract research, drug development, and manufacturing within a single organization.
It’s About Time
The trusted clinical research partner to accelerate drug discoveries, development and the path to commercialization.
How to Fast-Track Clinical Research Timelines
Speed is critical at every stage of drug development. Here’s how to overcome slowdowns and accelerate clinical research timelines.
Beat the clock in clinical development functions
Discover how an FSP model can optimize a follow-the-sun approach in this Pharmaceutical Outsourcing article
Five keys to successfully implement functional service partnerships
Read more about how FSP models help meet demanding timelines
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