Insights

Home/Insights
29 07, 2019

Overcoming Four Common Challenges in Multicenter Research

2019-08-01T13:38:11-04:00

Efficiently managing multicenter clinical trials is an essential capability of the modern research center. Complex protocols often require diverse subjects spread across a vast network of research sites - increasing pressure on the coordinating center to streamline operations, maintain oversight, and avoid compliance risks. While the challenges of managing multicenter trials is unique for [...]

Overcoming Four Common Challenges in Multicenter Research2019-08-01T13:38:11-04:00
26 06, 2019

Technology in Multicenter Clinical Trials

2019-08-02T11:34:14-04:00

Are you part of a multicenter clinical trial? If not, you may be soon. Multicenter trials, where a sponsor or CRO relies on a highly developed coordinating center to manage a network of sites, continue to gain popularity among sponsors looking to accelerate study timeline and reduce development costs. This growth is in direct [...]

Technology in Multicenter Clinical Trials2019-08-02T11:34:14-04:00
22 04, 2019

FDA: Technology’s Value in a World of Precision Medicine and Research

2020-01-14T09:13:08-05:00

Over the course of the past 10 years, significant advancements have been made in clinical research. Personalized medicine, immunotherapies and genomic testing have equipped researchers with the tools necessary to identify the biological causation of diseases and to target treatments accordingly. Yet in the face of therapeutic innovation, clinical trial operations have remained old [...]

FDA: Technology’s Value in a World of Precision Medicine and Research2020-01-14T09:13:08-05:00
27 03, 2019

ALCOA-C in Clinical Trial Electronic Document Management

2020-03-15T19:42:15-04:00

Good documentation is vital to good clinical research. As the saying goes, “If it isn’t documented, it doesn’t exist”. In fact, one of the most common inspection findings in investigator site inspections is the lack of reliable, accurate, and adequate source documentation. Failure to maintain adequate and accurate case histories that record all observations [...]

ALCOA-C in Clinical Trial Electronic Document Management2020-03-15T19:42:15-04:00
28 12, 2018

Thank you for a great 2018!

2019-08-02T15:47:21-04:00

What a great year at Florence! As we look back and celebrate all that has happened this year on our mission to advance research, we thank you for being a part of the Florence family. We are excited to share some of our highlights with you. Over 2,500 Research Teams added in 2018! Research [...]

Thank you for a great 2018!2019-08-02T15:47:21-04:00
19 12, 2018

Key Expectations of Clinical Trial Operations Leaders in 2019

2019-08-02T15:47:54-04:00

Today’s clinical trial operations leaders are in a challenging and expanding role. You are expected to increase study capacity, manage more complex trial protocols, accelerate study startup, and ensure timely sponsor collaboration - all while remaining hamstrung by limited resources, siloed data, stronger regulations, changing sponsor demands, and a growing site footprint. Clinical [...]

Key Expectations of Clinical Trial Operations Leaders in 20192019-08-02T15:47:54-04:00
12 12, 2018

Planning for 2019: Clinical Trial Site Industry Events

2019-08-02T15:48:30-04:00

Attending industry events is an excellent way to master new skills, keep a pulse on trends, learn best practices from other research sites, discover innovative technology transforming clinical trials, and network with your peers. Below are the clinical trial site industry events, conferences, and trade shows Florence is partnering with during 2019. We look [...]

Planning for 2019: Clinical Trial Site Industry Events2019-08-02T15:48:30-04:00
12 09, 2018

Ten Ways Florence eBinders™ Accelerates Study Startup

2020-01-14T09:15:06-05:00

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 Startup2020-01-14T09:15:06-05:00
15 05, 2018

10 Superpowers of Clinical Trial Leaders

2019-08-02T15:59:52-04:00

While helping over 2,000 research teams migrate Florence eBinders for eRegulatory, we've encountered people who have become "superheroes" in managing the workflow of regulatory and source documents at their site. In working closely with them to take what they are doing now and move it to a streamlined digital workflow, we've identified ten types of these "superheroes" and [...]

10 Superpowers of Clinical Trial Leaders2019-08-02T15:59:52-04:00