Resources

“I have too many systems!” | The Top 5 Integrations You Need

2018-01-12T12:33:03+00:00

New technology should accelerate your studies, however, for many research sites new technologies end up adding complex and redundant processes for your team. Avoiding these additional processes requires tight integration. Moreover, many technology solutions claim to have integrations but it is important to ask exactly how they will integrate with the systems you are [...]

“I have too many systems!” | The Top 5 Integrations You Need 2018-01-12T12:33:03+00:00

Florence at TMF Summit 2018

2018-01-04T22:29:14+00:00

Attending the Trial Master File Summit 2018 in Orlando January 16-18? Make the most of your trip by learning how Florence eBinders eISF + eTMF will accelerate your studies and streamline access to your sites. Our team will be demoing our innovative and leading solution for simplifying and advancing clinical research—trusted by more than 2,000 [...]

Florence at TMF Summit 2018 2018-01-04T22:29:14+00:00

Roadmap to eRegulatory: Define Eight Critical Workflows

2017-10-26T15:59:29+00:00

Transitioning to an eRegulatory platform is full of benefits; accelerated study startup, centralized document management, the ability to review and sign documents anywhere, easy task management, remote monitoring, and more. After hundreds of successful site implementations, our team has developed a complete guide for clinical research sites and centers planning for eRegulatory, available here. Download [...]

Roadmap to eRegulatory: Define Eight Critical Workflows 2017-10-26T15:59:29+00:00

Your Roadmap to eRegulatory: Establishing Goals

2017-10-26T15:58:52+00:00

Transitioning to an eRegulatory platform is full of benefits; accelerated study startup, centralized document management, the ability to review and sign documents anywhere, easy task management, remote monitoring, and more. However, nearly 80% of the sites we talk to have not yet implemented this time and cost savings workflow - why is this? The simple [...]

Your Roadmap to eRegulatory: Establishing Goals 2017-10-26T15:58:52+00:00

5 Ways To Engage Clinical Trial Sites With Technology

2017-07-14T15:43:32+00:00

As Featured in Clinical Leader, July 13 2017 Clinical research has a reputation for being notoriously slow to adopt new technologies. This should come as no surprise to those in the industry, since we operate in a highly regulated environment. We’re generally skeptical about technology for three main reasons: Potential data security and compliance issues [...]

5 Ways To Engage Clinical Trial Sites With Technology 2017-07-14T15:43:32+00:00

eClinical tools to dClinical tools

2017-07-14T15:44:35+00:00

Gartner’s Michael Shanler was one of the first to recognize the trend of dClinical. He noticed that a new generation of software vendors was emerging who handled project management and reporting in a new way. Florence agrees with Michael’s observation, which is why we’re building tools that align with a dClinical approach. An abbreviated history [...]

eClinical tools to dClinical tools 2017-07-14T15:44:35+00:00