Study Startup

/Study Startup
12 09, 2018

Ten Ways Florence eBinders Accelerates Study Startup

2018-09-26T14:47:07+00:00

Moving to an eRegulatory/eSource solution generates measurable impact on clinical trial study startup timelines. Research teams reduce startup time by as much as 40% through harnessing the built-in features of eBinders combined with excellent standard operating procedures. Below are the top ten features more than 3,000 research teams are using to accelerate their study [...]

Ten Ways Florence eBinders Accelerates Study Startup2018-09-26T14:47:07+00:00
7 08, 2018

Ten Must-Have Capabilities When Evaluating eRegulatory Platforms

2018-08-07T11:39:27+00:00

Successfully transitioning your team to an eRegulatory solution, while avoiding costly compliance mistakes and realizing true time-saving benefits, requires careful evaluation of potential platforms. After helping thousands of research teams implement eRegulatory, our team has put together these ten essential capabilities to look for when evaluating solutions. You can download our full Guide to Selecting [...]

Ten Must-Have Capabilities When Evaluating eRegulatory Platforms2018-08-07T11:39:27+00:00
12 03, 2018

Cancer Research Is Accelerating, but We Can Do Better

2018-03-12T10:48:40+00:00

The rate of cancer death has been decreasing, and people are living longer with cancer than ever before. Approximately 64% of US patients diagnosed with cancer in 2005 have lived 10 years or more beyond diagnosis, up from 35% for those diagnosed in 1975. — American Society of Clinical Oncology Cancer Advances Report, 2018. [...]

Cancer Research Is Accelerating, but We Can Do Better2018-03-12T10:48:40+00:00