23 04, 2018
27 03, 2018
The Impact of Remote Monitoring on CRAs | Central Monitoring Summit
Ryan Jones2018-03-27T21:24:16-04:00While presenting at Central Monitoring Summit 2018, Elizabeth Robinson of Horizon Pharma shared a strong data point: In the coming years, Clinical Research Associates (CRAs) will experience more change to their jobs than any other research profession (2017 Applied Clinical Trials survey). This statement spurred a conversation amongst the room about what will change [...]
19 03, 2018
[Infographic] Launching eSignatures in Clinical Trials while Avoiding Part 11 Risks
Florence Team2018-06-18T15:25:39-04:00Electronic signatures, eSignatures, are continuing to gain momentum in the clinical trial landscape. The immediate benefits of eSignatures are clear - your team can eliminate the printing of most regulatory documents, chasing signers, and scanning and faxing files.However, recent advances in purpose-built solutions employ eSignatures for far more than these basic benefits. Solutions in eRegulatory [...]
15 03, 2018
7 02, 2018
Innovations | The time is now for eRegulatory and eSource
Florence Team2018-04-06T22:30:42-04:00Innovation matters in Clinical Research… The adoption of new technology, in any industry, follows a familiar cycle outlined by Geoffrey Moore in his book Crossing the Chasm, Innovators: Innovators are the first individuals to adopt an innovation. These individuals/teams are willing to take a risk to help advance a solution. Early Adopters: These are the [...]
31 01, 2018
16 01, 2018
8 01, 2018
“I have too many systems!” | The Top 5 Integrations You Need
Florence Team2018-01-12T12:33:03-04:00New 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 [...]
7 11, 2017
25 10, 2017
Roadmap to eRegulatory: Define Eight Critical Workflows
Florence Team2017-10-26T15:59:29-04:00Transitioning 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 [...]