New! Electronic Investigator-Controlled Site File (eISF)
Increase Efficiency, Lower Costs, and Reduce Site Visits
Provide clinical investigators with the ability to electronically file their clinical documents efficiently. Now study monitors can focus their time on helping your sites succeed, rather than chasing documents.Learn more
Where partnering works
The pressure is on
There is a paradigm shift happening across life science organizations and business process innovation is at the heart of it. The blockbuster drug has gone, but the processes and costs have remained.
Enter the latest iteration of agile partnerships – for the new era of personalized medicine. From simple process outsourcing to large sponsors working together to develop drugs – cost effectively. Your partnerships will define your success in the future.
You need to be able to share information securely, organize content centrally, manage access to content and meet regulatory compliance requirements – effortlessly.
Intralinks puts you firmly in control, without compromising your ability to simply get work done.
Who we work with:
THE TOP 20 pharmaceutical companies
THE TOP 10 biotech companies
THE TOP 5 CROs
60,000 investigative sites around the globe
Over 200 biopharmaceutical companies
Come and meet
- PCT (Partnerships in Clinical Trials)
- Advances in Clinical Technology
- eClinical Forum
- BayBio Lunch & Learn
- 5th Annual SCOPE Summit
- September 18, 2014 — eISF Webcast
- 11AM New York/4PM London, Speaker: Andrew Mitchell, Director LS Strategy and Product Marketing
- "Remote monitoring of Investigator Site Files (regulatory Blinders) and Source Documents"
- June 5, 2014 — Webcast
- May 8, 2014 — Webcast