“Our staff and our technology allowed us to quickly adapt to the new environment without missing a beat.”
"Studies involving genetically engineered materials have the potential to bring incredible options to patients but involve greater complexity to operationalize. It’s imperative for sponsors, CROs, and vendor partners to work together in innovative ways to complete these trials in a timely fashion. This study was a high-profile trial for the sponsor and Parexel, requiring detailed preparation and critical path management. We worked diligently with our client success partners at Advarra to de-risk startup by pre-planning the site activation strategy, selecting sites from the Gene Therapy ReadyTM list, and pre-reviewing most of the IRB/ IBC site applications for potential issues early in the process. When it was time to review and activate sites, Advarra held 68 IBC meetings in one week to approve our first batch of sites. IRB review was right behind, with nearly all 145+ sites reviewed and approved within a couple of weeks. Advarra’s IBC services provided the full-service integration with the IRB we were seeking. We achieved the startup targets for sites utilizing the central IRB/IBC review service, the sponsor was delighted, and the research protocol was up and running in an impressive timeframe."
Medrio has offered an integrated eClinical Software as a Service (SaaS) platform with a fully hosted Electronic Data Capture (EDC) system that drastically reduces study timelines and costs by putting study managers in control of their studies. By enabling studies to be built completely online without the need for any custom development, Medrio eClinical software allows studies to be ready in days instead of weeks. Medrio's hundreds of customers span across the world and include 12 of the top 20 global biopharmaceutical companies and 3 of the top 10 CROs.
Teckro connects investigators and research site staff, sponsors and monitors with both each other, and the critical study information they need, when they need it. A digital clinical trial hub of content, communication and collaboration, Teckro transforms the clinical trial protocol from a static document into a critical data source for engagement and trial conduct. Global pharmaceuticals and emerging biotechnology companies alike rely on Teckro for all trial phases and therapeutic areas. Headquartered in Limerick, Ireland, Teckro has locations across Europe and the United States.
Veeva Systems is a leader in cloud-based software for the global life sciences industry. Committed to innovation, product excellence, and customer success, Veeva has more than 450+ customers, ranging from the world's largest pharmaceutical companies to emerging biotechs. Veeva is headquartered in the San Francisco Bay Area, with offices in Europe, Asia, and Latin America.