StudyOrganizer – Your Complimentary Study Management Assistant

9 11, 2023

Unlocking Efficiency with VersaTrial: Your Essential Tool for Simplifying Study Operations

2023-11-09T15:38:31-05:00

ON-DEMAND WEBINAR Unlocking Efficiency with VersaTrial: Your Essential Tool for Simplifying Study Operations Are you tired of juggling countless documents, passwords, and sponsor contacts to manage your studies? Discover how the VersaTrial Study Organizer, a cutting-edge, free, and easy-to-use tool, is transforming the way research sites streamline their study management. Designed for clinical [...]

Unlocking Efficiency with VersaTrial: Your Essential Tool for Simplifying Study Operations2023-11-09T15:38:31-05:00
18 02, 2020

How the MAGI eISF Reference Model Will Impact Your Work

2023-04-16T23:19:01-04:00

eISF Reference Model Overview You’ve likely heard that the MAGI Global eISF / eReg Binder Reference Model Version 0.9 is open and available for review. By now, you may be wondering what’s next for me and my organization? Our representative on the MAGI eISF Reference Model Steering Committee, Jordan Tapley, walks us through [...]

How the MAGI eISF Reference Model Will Impact Your Work2023-04-16T23:19:01-04:00
14 08, 2019

Webinar Recording | eTMF + eISF Integrations: Why and Why Now?

2019-08-14T11:03:06-04:00

Watch: eTMF + eISF Integration - Why and Why Now? Discover how it is now possible to directly integrate the eTMF and the Research Site eISF to accelerate research by connecting in a unified digital ecosystem. The use of electronic documentation in clinical trials, both at the site (eISF) and the [...]

Webinar Recording | eTMF + eISF Integrations: Why and Why Now?2019-08-14T11:03:06-04:00
29 07, 2019

Overcoming Four Common Challenges in Multicenter Research

2023-05-03T21:57:47-04:00

Overcoming 4 Challenges in Multicenter Clinical Trials 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 [...]

Overcoming Four Common Challenges in Multicenter Research2023-05-03T21:57:47-04:00
17 07, 2019

Webinar Recording | Managing Multi-Center Clinical Trials

2020-05-12T16:39:21-04:00

Webinar Recording: Best Practices for Managing Multicenter Research As the number of multicenter trials continues to grow, it is essential that coordinating centers begin thinking about their technology like a sponsor. This is especially important when it comes to the management of your data and documents. Leading coordinating centers are now [...]

Webinar Recording | Managing Multi-Center Clinical Trials2020-05-12T16:39:21-04:00
26 06, 2019

Technology in Multicenter Clinical Trials

2023-05-03T21:58:23-04:00

Managing and Organizing Multicenter Clinical Trials with Technology Are you part of a multicenter clinical trial? If not, you may be soon. Multicenter clinical 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 [...]

Technology in Multicenter Clinical Trials2023-05-03T21:58:23-04:00
13 03, 2019

Webinar | Multi-center Clinical Research Management

2020-05-12T17:06:09-04:00

Watch: Best Practices for Multicenter Research Management with Technology Learn best practices, tips, and tricks for managing multicenter clinical trials with technology. Multicenter research introduces unique challenges and bottlenecks for clinical trial leaders who are expected to manage studies across sites. To avoid study delays and compliance risks when managing multi-site [...]

Webinar | Multi-center Clinical Research Management2020-05-12T17:06:09-04:00
12 02, 2019

5 Key Advantages of eRegulatory

2021-05-20T11:37:39-04:00

Over 75% of clinical trial sites who have not yet adopted eRegulatory plan to do so in 2019. Why? In addition to growing industry pressure from sponsors who expect a digital site infrastructure, trial sites with eRegulatory platforms are introducing key advantages over those sites without eReg. What are those advantages? Download Five Key Benefits [...]

5 Key Advantages of eRegulatory2021-05-20T11:37:39-04:00
18 01, 2019

How Lauren Begnaud Transitioned 65 Sites to eRegulatory at US Oncology

2021-05-20T11:21:24-04:00

In this interview, we talked with Lauren Begnaud, Manager of Regulatory Affairs at the US Oncology Network, to discover how she successfully migrated 65 trial sites, 400 studies, and 2,000 Investigators and Support Staff to Florence eBinders for eRegulatory. Lauren has over 10 years of experience in the clinical research field and has successfully [...]

How Lauren Begnaud Transitioned 65 Sites to eRegulatory at US Oncology2021-05-20T11:21:24-04:00
19 12, 2018

Key Expectations of Clinical Trial Operations Leaders in 2019

2021-05-20T10:55:14-04:00

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 20192021-05-20T10:55:14-04:00
12 09, 2018

Ten Ways Florence eBinders™ Accelerates Study Startup

2021-05-20T10:36:27-04:00

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 Startup2021-05-20T10:36:27-04:00
7 08, 2018

Ten Must-Have Capabilities When Evaluating eRegulatory Platforms

2021-05-20T10:17:46-04:00

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 Platforms2021-05-20T10:17:46-04:00
14 06, 2018

Webinar | Avoiding Digital Site Surprises

2019-08-02T15:56:28-04:00

Recorded Webinar: Avoiding Digital Site Surprises Odds are that your CRA team is already logging into electronic investigator site files at some of your sites. Now what? View this on-demand webinar to learn how leading sponsors and CROs are taking advantage of digital platforms at trial sites. We explore the how your [...]

Webinar | Avoiding Digital Site Surprises2019-08-02T15:56:28-04:00
13 06, 2018

How to Avoid the Top 5 Clinical Trial FDA Inspection Failures

2021-05-20T10:00:32-04:00

Your heart begins beating faster and sweat begins forming on your forehead - the FDA is calling. Many things can trigger an FDA inspection - most falling into routine study-related visits, while some are "for cause," stemming from complaints or sponsor concerns. Sites that have a new drug application will most likely experience an FDA inspection. [...]

How to Avoid the Top 5 Clinical Trial FDA Inspection Failures2021-05-20T10:00:32-04:00
4 06, 2018

Webinar | Surviving an FDA Inspection with eRegulatory

2019-08-02T15:57:14-04:00

On-Demand Webinar: Surviving an FDA Inspection with eRegulatory In this recorded webinar our panel of experts from Florence and LMK Clinical Research discuss how an FDA inspection works with eRegulatory, what the FDA is looking for, and how to prepare your site for a successful inspection. [...]

Webinar | Surviving an FDA Inspection with eRegulatory2019-08-02T15:57:14-04:00
15 05, 2018

10 Superpowers of Clinical Trial Leaders

2021-07-27T20:20:36-04:00

While helping over 10,000 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" [...]

10 Superpowers of Clinical Trial Leaders2021-07-27T20:20:36-04:00
1 05, 2018

Webinar | Solving Clinical Trial Inefficiencies with eRegulatory

2022-10-20T11:50:33-04:00

Webinar: Solving Clinical Trial Inefficiencies with eRegulatory In this on-demand webinar our team examines how leading clinical trial sites are solving clinical trial operation inefficiencies with eRegulatory. Introducing eRegulatory into clinical trial trials is proving to deliver real operational improvements with a measurable impact on efficiency for thousands of trial sites. [...]

Webinar | Solving Clinical Trial Inefficiencies with eRegulatory2022-10-20T11:50:33-04:00
1 05, 2018

5 Things to Know about Blockchain and Clinical Trials

2021-05-20T09:44:33-04:00

“Blockchain will change the world!” This is the common message found in search engines and blog posts across the internet. But really, how many times have you heard this message before? It seems that a new, life-changing technology launches daily, so when should you actually pay attention to one of these “breakthroughs”? The answer [...]

5 Things to Know about Blockchain and Clinical Trials2021-05-20T09:44:33-04:00
7 02, 2018

Innovations | The time is now for eRegulatory and eSource

2021-05-19T18:40:00-04:00

Innovation 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 [...]

Innovations | The time is now for eRegulatory and eSource2021-05-19T18:40:00-04:00
8 01, 2018

“I have too many systems!” | The Top 4 Integrations You Need

2021-05-19T18:31:00-04:00

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 4 Integrations You Need2021-05-19T18:31:00-04:00
25 10, 2017

Your Roadmap to eRegulatory: Define Eight Critical Workflows

2021-05-19T18:25:03-04:00

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. [...]

Your Roadmap to eRegulatory: Define Eight Critical Workflows2021-05-19T18:25:03-04:00
14 07, 2017

5 Ways To Engage Clinical Trial Sites With Technology

2021-05-19T17:49:13-04:00

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 [...]

5 Ways To Engage Clinical Trial Sites With Technology2021-05-19T17:49:13-04:00
30 03, 2017

Can I control access with electronic binders?

2021-05-19T17:37:27-04:00

You’ve decided to make the transition from papers to digital. Your sponsor is on board. You’ve organized your binder and folder structure templates. Now what? It’s time to configure access by setting up roles and permissions. Not sure where to start? Here’s a quick guide to managing your team digitally. Wait, I never had [...]

Can I control access with electronic binders?2021-05-19T17:37:27-04:00
24 02, 2017

What’s Your eRegulatory Strategy?

2021-05-19T17:03:28-04:00

What’s your eRegulatory Strategy? In the last year we’ve met with dozens of research teams to discuss this question. In the process, we've discovered that moving to an eRegulatory platform is much more than moving from paper to digital documents. Formulating a site-wide strategy for eRegulatory means considering 1) the benefits you seek, 2) [...]

What’s Your eRegulatory Strategy?2021-05-19T17:03:28-04:00
19 12, 2016

What if I get audited?

2021-05-19T16:56:56-04:00

A common question many teams ask as they face the transition to digital study documents is, “What if I get audited?” Inspections evoke fear because negative audit findings significantly impact everyone. Areas of high risk include missing documents, accurate delegation of authority logs, reporting delays, and inadequate monitoring or PI oversight. Given these risks, some [...]

What if I get audited?2021-05-19T16:56:56-04:00
15 12, 2016

“My PIs are super busy and unable to try new things! How can I convince them to try eBinders?”

2021-05-19T16:50:18-04:00

Research protocol complexity is increasing and trial volumes are growing. The result - sites are struggling to take on more with the same team. Physicians and research teams are overwhelmed with cumbersome documentation and oversight requirements spread out across multiple locations. Workload imbalance and audit risk anxiety has led to turnover – exacerbating the [...]

“My PIs are super busy and unable to try new things! How can I convince them to try eBinders?”2021-05-19T16:50:18-04:00
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