Transforming CMC Generation Through Automation and Structured Content
Unlock the potential for unprecedented efficiency and cost savings in pharmaceutical and biotech companies with BIOVIA's Structured Document Manager and…
Unlock the potential for unprecedented efficiency and cost savings in pharmaceutical and biotech companies with BIOVIA's Structured Document Manager and…
Authoring Chemistry, Manufacturing and Controls (CMC) dossiers is a complex process. Information is collected from the early development to the…
Often patients who want to be proactive about treatments for their conditions will seek out medical trials. Unfortunately, there are…
Clinical trials have the potential to take up a lot of time for doctors, who also have to find a…
Sponsors running clinical trials want to provide both patients and sites with the best experience possible when conducting trials. Medidata…
Patient centricity emphasizes prioritizing patients' experiences and outcomes, yet a universally accepted definition and standardized approach for patient-centric trials remain…
The competitive race to develop and launch new therapies faces challenges, including lengthy timelines, increased costs, and low drug approval…
Lack of diversity in clinical trials has been a long-standing issue, and one with extensive implications. It can not only…