New PROPEL Survey Feature

In the fast-paced world of clinical trials, feasibility surveys have become a crucial step in the process. These surveys help researchers determine the viability of their trials and ensure that all the necessary resources and capabilities are in place. However, it is important to recognize that surveys have the potential to be powerful tools in various other aspects of clinical research. Building relationships, understanding site capabilities, and gathering feedback are just a few of the areas where surveys can prove to be invaluable. 

Surveys are an incredibly powerful tool, allowing researchers to collect feedback and insights from a wide range of recipients. Whether it’s gathering information from sites within your network, potential vendors, patients, or investigators, surveys can provide valuable data that can inform important decisions. 

PROPEL Enterprise’s new Survey Feature is an exciting development for the clinical trial industry. With this innovative tool, researchers can create and distribute surveys directly within the platform, reaching a large audience and gaining valuable data in a streamlined and efficient manner. 

How It Works 

PROPEL Enterprise‘s new Survey Feature functionality (GIF). 

Quickly create and send surveys directly within PROPEL to LYNK users or external email lists. Use pre-built templates, import existing questions, or create a survey from scratch with PROPEL’s easy-to-use interface. For ease of tracking, you can also associate your survey with a specific trial, contact, or account. 

Once a survey is sent, PROPEL will automatically collect all timing and response data in one place for easy monitoring and reporting – giving you real-time visibility into who has completed a survey, who hasn’t, and who stopped part-way through. But the feature doesn’t stop there – eliminate endless follow-up emails with automated alerts and reminders. 

Instead of relying on multiple programs and websites to send and track surveys, PROPEL provides a closed-loop system allowing you to make surveys, send them out, and to get in-depth analytics on responses and timing.  

For Any Kind of Survey 

Survey Feature interface. 

PROPEL’s new feature aims to transform and streamline the survey process – from feasibility and CSAT to PI onboarding, equipment management, and beyond! Surveys can be as general or specific as you want and for any use case under the sun. Want to know what kind of studies sites are looking for? Need to follow-up with a site or PI about a recent onboarding? PROPEL’s new Survey Feature is here to help! 

Ready to see how Devana Solutions continues to revolutionize how clinical research professionals gather and analyze feedback? Schedule a demo today! 

Devana Solutions  

Devana Solutions is an innovative cloud-based clinical trial software company that supports real-time collaboration between central research operations professionals and decentralized clinicians serving patients in diverse communities. Devana Solutions bridges the technology access and data divide by seamlessly and securely connecting decentralized researchers to other mission-critical clinical trials systems.  

Let us show you in more detail what Better Data, Better Decisions, Better Outcomes could do for your clinical trial processes. Book a demo with Devana Solutions today to learn about our cloud-based data analytics clinical trial software for the clinical trials industry that integrates seamlessly with CTMS and other key systems to keep success in the crosshairs.  

Optimize Clinical Trials with Automated Workflows and Data Analytics

In a world that has become increasingly focused on the capabilities of artificial intelligence (AI), it’s hard to imagine a future without most industries being impacted. But while an AI for every niche business need may still be in the future, advanced technologies offering increased efficiency, quality, and time and cost savings are already here. 

Designed specifically for the clinical trials industry, PROPEL’s category-defining technology provides automated workflows and advanced data analytics throughout the entire clinical trial process. 

Automated Workflows 

PROPEL is a cloud-based technology that helps research organizations save time and money through automating clinical trial workflows from initial study lead to trial completion. Providing a single platform for securely storing and managing all your clinical trial data, PROPEL offers full visibility into workflows and next steps across your organization – saving time and reducing risk. With PROPEL, you can accelerate pre-award milestone completion with automated queries, real-time chat threads, and smart workflows. Plus, create and assign custom tasks and alerts to keep things from slipping through the cracks. 

Some aspects of clinical trials are harder to speed up than others. Screening and recruiting patients often takes the longest, requiring more manpower and effort. By accelerating the tasks you can speed up, you can save time for more labor-intensive tasks. PROPEL’s streamlined platform eliminates many repetitive tasks, including data entry into multiple systems and countless calls and emails used to query and update sites. For example, PROPEL’s Outlook integration provides AI-enhanced automatic email capture and attachment, linking relevant information and documentation to an associated trial.  

A single shared system for all data, documents, and communication, PROPEL is the core to any clinical trial tech stack. 

Advanced Data Analytics 

PROPEL provides organizations with the ability to analyze trial and site performance data in real time, allowing you to choose top performing sites and investigators for your study. View full study pipelines and trial stages across all your sites, enabling you to compare progress and take action on any bottlenecks. Quickly make informed decisions based on accurate, timely data.  

PROPEL homepage and Business Development Dashboard.

With access to both real-time and historical data and the ability to analyze and visualize it automatically with custom dashboards and reports, you’ll gain powerful insights into potential outcomes of current and future trials. Right away, you’ll be able to establish benchmarks to measure efficiency, timing metrics, and overall improvement. See patterns appear within the industry and your own organization, allowing you to capitalize on trends and areas of increased demand.  

Seamless integrations with CTMS and other key systems provide you with holistic views into your entire clinical trial process, saving you time and money and increasing your chances of a successful outcome. As trials progress and updates happen across the system, PROPEL automatically captures timing metrics generated on the platform or via integration, providing leadership and study teams with real-time data they can take immediate action on. 

By eliminating repetitive tasks, streamlining workflows, and providing enhanced data analysis, more time can be spent by staff on specialized tasks and patient-centric duties. The end goal of any clinical trial is to get new and better treatments to market faster, and PROPEL’s automations and optimizations can help you get there.  

Don’t wait, schedule a demo and start accelerating your clinical trial processes today! 

Devana Solutions  

Devana Solutions is an innovative cloud-based clinical trial software company that supports real-time collaboration between central research operations professionals and decentralized clinicians serving patients in diverse communities. Devana Solutions even bridges the technology access and data divide by seamlessly and securely connecting decentralized researchers to other mission-critical clinical trials systems.  

Let us show you in more detail what Better Data, Better Decisions, Better Outcomes could do for your clinical trial processes. Book a demo with Devana Solutions today to learn about our cloud-based data analytics clinical trial software for the clinical trials industry that integrates seamlessly with CTMS and other key systems to keep success in the crosshairs.  

Gain Crucial Trial Oversight with Clinical Trial Software for AMCs

By design, clinical trials are a long and complicated process involving a seemingly endless number of moving parts. It can be difficult to manage everything effectively, especially with the rise of decentralized study teams and more complex trial designs and protocols. For Academic Medical Centers (AMCs) in particular, project management across the entire clinical trial process often proves to be a time-intensive challenge.  

Devana Solutions’ category-defining PROPEL technology offers real-time oversight into trial status, custom integrations, and powerful collaboration tools. Serving as the central hub in any given clinical trial tech stack, PROPEL combines all the key data in one place—providing AMCs with total performance transparency, automated workflows, and reduced workloads overall.  

Project Management and Trial Oversight 

PROPEL Contract % by Trial Report

PROPEL is a powerful project management tool that enables teams to establish improved workflows throughout the entire clinical trial process. Promote buy-in and accountability with transparency into trial status, outstanding tasks, enrollment goals, and performance expectations both organization-wide and for each individual study team. View at a glance which trials are proceeding on schedule, and which are not – allowing for timely interventions to get you back on track.   

With PROPEL, AMCs can track enrollment, activity, timing, and performance based on trial, study team, sponsor, and more. Create customized dashboards and reports using real-time data for powerful metrics and improved trial management. With oversight into every aspect of clinical trials in the system, PROPEL makes it easy for teams to give guidance and resources where needed.   

Study teams also gain visibility and accountability into the study startup progress, enrollment performance goals, and overall trial status. PROPEL allows them to respond to notifications of the latest trial opportunities, along with other task alerts tied to specific trials. Threaded chat conversations streamline communication and allow for real-time collaboration and document sharing. Connect teams no matter their location with PROPEL.  

Seamless Integrations 

With the wide array of disjointed technology such as CTMS, IRB, contracts and budgets, grant management, and more, PROPEL’s open API gives AMCs the power to seamlessly integrate with the tools their team is already using. Integrations with mission-critical systems allow data to flow and synchronize across all platforms, providing powerful oversight for central research teams. Paired with PROPEL’s custom dashboards and reports, cross-platform data can be easily shared with key stakeholders anytime. 

Acting as the hub of the clinical trial tech stack, PROPEL’s custom integrations bring together all the clinical trial data from IRB systems, contract and budget programs, regulatory systems, and beyond—all in one place. By tying together disparate systems in one centralized and easy-to-use platform, AMCs can eliminate duplicate data entry and boost trial cycle times.  

Want to learn more? Download the PROPEL sell sheet 

Devana Solutions  

Devana Solutions is an innovative cloud-based clinical trial software company that supports real-time collaboration between central research operations professionals and decentralized clinicians serving patients in diverse communities. Devana Solutions even bridges the technology access and data divide by seamlessly and securely connecting decentralized researchers to other mission-critical clinical trials systems.  

Let us show you in more detail what Better Data, Better Decisions, Better Outcomes could do for your clinical trial processes. Book a demo with Devana Solutions today to learn about our cloud-based data analytics clinical trial software for the clinical trials industry that integrates seamlessly with CTMS and other key systems to keep success in the crosshairs.  

PROPEL Spring ’23 Update

Get ready for an exhilarating update to PROPEL! The Spring ’23 Update brings a plethora of enhancements, refinements, and additions to the platform designed to improve and streamline the user experience system wide with a heavy focus on Trials and Trial Management.  

PROPEL’s latest release is all about optimizing glanceability and improving workflows while prioritizing the information that means the most, from harmonized field names to a new glossary for credentials and the release of Trialstones. The theme underlining the entire release can be summed up as “Trials” – which have been given a complete makeover, including new Trialstones, streamlined tabs and fields, and a progress bar to keep track of trial status. 

What’s New? 

The user interface (UI) has been updated and enhanced across several areas of the platform so everything can be quickly absorbed at a glance. A key part of the updated UI is the new progress bar, which clearly shows what stage a trial is currently in. New, more visually compelling monitoring tiles have replaced checklists in various places, making content more scannable and insights digestible. See below for a look at the new real-time progress bar and pre-award Trialstones tiles.  

PROPEL Trial page with new progress bar and pre-award Trialstones.

What’s a Trialstone, you ask? Pre- and post-award trial milestones are now known as Trialstones throughout the platform. When sites complete Trialstones such as CDA Executed or PSV Complete, this information will be updated across the system – including advancing the trial stage in the new progress bar. Users can track and manage Trialstones directly from any trial page within PROPEL for improved workflows. With the new update, Trialstones can also be updated for multiple sites at once to save time.  

Another great new feature coming in this update is that trials can now be marked as high priority. Making a trial high priority adds a red star to the list view, clearly calling out trials which have been flagged. This new feature allows central team users to delineate which opportunities and trials sites should focus on first. 

We’ve only covered some of the broader highlights, but the Spring 2023 Update brings a lot of exciting new quality of life changes to PROPEL and LYNK. Full release notes and training materials have already been made available to our existing partner-clients. If you’re interested in learning more, please contact us today and we’d be happy to give you a demo of our game-changing platform. 

Devana’s product development pipeline has more exciting updates and features coming soon, so stay tuned!  

Devana Solutions  

Devana Solutions is an innovative cloud-based clinical trial software company that supports real-time collaboration between central research operations professionals and decentralized clinicians serving patients in diverse communities. Devana Solutions even bridges the technology access and data divide by seamlessly and securely connecting decentralized researchers to other mission-critical clinical trials systems.  

Let us show you in more detail what Better Data, Better Decisions, Better Outcomes could do for your clinical trial processes. Book a demo with Devana Solutions today to learn about our cloud-based data analytics clinical trial software for the clinical trials industry that integrates seamlessly with CTMS and other key systems to keep success in the crosshairs.  

Accelerate Study Cycle Times with Clinical Trial Software for CROs

In our post-pandemic world, contract research organizations (CROs) face more challenges than ever. With greater competition, market consolidation, and a growing emphasis on site empowerment, the CRO market is in a state of flux. Only those willing to be flexible as they apply learnings from the COVID-19 pandemic and its aftermath are likely to come out ahead.   

One of the key takeaways from the COVID-19 pandemic applied throughout the clinical trial industry is to invest in mission-critical technology. Devana Solutions’ category-defining PROPEL platform offers improved site selection, real-time communication, and site collaboration. PROPEL provides process and performance transparency while automating workflows, accelerating cycle times, and reducing the overall workload for CROs and sites. 

Improved Site Selection 

PROPEL Site Query Functionality

CROs have long relied on manual, time-consuming processes to identify the most suitable sites for new clinical trials. With PROPEL, we’ve eliminated this outdated approach. 

PROPEL enables CROs to perform targeted queries to determine suitable sites for new trials. Find the most effective sites in real-time by digitally querying site capabilities based on therapeutic expertise, physical site facilities, investigator and staff certifications, and more. PROPEL automatically stores site and investigator performance and capabilities data to share with sponsors or use for future trials.  

With PROPEL, CROs can be confident in the sites they’ve selected when reporting back to sponsors with progress updates. 

Real-Time Collaboration 

When you have a clinical trial underway, it’s important to have a tool that makes it easy for you to share information with sites—and receive real-time responses. 

Forget endless follow-up emails, calls, and meetings. Instead, push out mass communications or individually tag relevant users or site teams, alerting them of new trial opportunities, updates, or queries. PROPEL’s threaded chat conversations allow CROs and sites to pose questions, share documents, and provide updates. Real-time feedback from sites, such as if there are too many inclusion/exclusion criteria or more realistic estimates for patient enrollment, can help CROs with sponsor bid defenses. Sites can also ask questions and share documents via the same channels—keeping everyone in the loop throughout the entire clinical trial process.  

With PROPEL, CROs also gain insights into other site organizations already using PROPEL, including two of the largest site networks and the largest site organization in the world. 

Performance Transparency 

 

PROPEL Site Activity Dashboard

When running clinical trials, you need to be able to track and analyze current and historical metrics. This is where PROPEL comes in. 

Tracking current and historical trial metrics with PROPEL’s dashboards and reports can help CROs win more sponsor bid defenses by quantifying past successes and showcasing real-time updates for trials currently running. Key data generated throughout the clinical trial process is automatically stored within PROPEL and can be accessed via custom reports and visualizations whenever needed. Know exactly how a trial progresses from site selection to completion with real-time data capture and analysis. Identify bottlenecks in terms of site responses, patient enrollment, and more so you can step in and provide targeted support where needed.  

Sharing the latest data anytime with stakeholders and sponsors is critical to accelerating cycle times and mitigating bottlenecks and risks.  

Want to learn more? Download the PROPEL sell sheet 

Devana Solutions  

Devana Solutions is an innovative cloud-based clinical trial software company that supports real-time collaboration between central research operations professionals and decentralized clinicians serving patients in diverse communities. Devana Solutions even bridges the technology access and data divide by seamlessly and securely connecting decentralized researchers to other mission-critical clinical trials systems.  

Let us show you in more detail what Better Data, Better Decisions, Better Outcomes could do for your clinical trial processes. Book a demo with Devana Solutions today to learn about our cloud-based data analytics clinical trial software for the clinical trials industry that integrates seamlessly with CTMS and other key systems to keep success in the crosshairs.  

3 Key Differences Between PROPEL and CTMS

High staff turnover and burnout have been trending topics in the clinical trials industry over the last year. The goal of successful clinical trials is to get new treatments to market as quickly and safely as possible; however, the process from study startup to study completion is lengthy, and staff turnover causes disruption. With the right technology, standard pre-enrollment steps can be streamlined, automated, and accelerated across your site or site network—ensuring business intelligence is neither overlooked nor forgotten as staffing situations change. 

Furthermore, speeding up the pre-enrollment process can help increase diversity in clinical trials by onboarding sites faster, making your organization look more attractive to sponsors and CROs. 

PROPEL vs. CTMS 

A traditional clinical trial management system (CTMS) is designed to manage patient recruitment, scheduling, and study finances. But if you’re only using a CTMS, it can be hard to proficiently track enrollment and site activity, trial opportunities, timing, and performance across your entire clinical trial operations.   

Fig.1 Unique within the clinical trials industry, PROPEL is an all-inclusive pipeline, startup, trial intelligence, and automation system.

Built for clinical trials, PROPEL is uniquely different from a CTMS. On average, site networks save almost 30 hours of time per week and increase revenue by 40% throughout the end-to-end clinical trial process with PROPEL’s improved workflows, study startup automation, and seamless integrations with popular CTMS and other mission-critical systems for end-to-end operational excellence. With PROPEL, information silos are replaced with organization-wide visibility into trial data and operations. While your CTMS is triggered at recruitment or post-enrollment, PROPEL is involved from initial pipeline management all the way through to study completion and analysis.  

1. Study Startup Automation  

PROPEL is a comprehensive solution that optimizes study startup and performance. Unlike a CTMS, our category-defining technology allows you to automate your pipeline of trials and your study startup. This allows users to seamlessly track and update milestones throughout the entire startup process. PROPEL transforms the pre-enrollment and study startup process in addition to providing wrap-around reporting every step of the way.   

2. Advanced Custom Analytics & Reporting (from initial pipeline management to study completion) 

Although CTMS includes metrics such as study enrollment, visit tracking, and protocol deviation logs, they do not include other essential insights that give you a comprehensive view of your organization. With PROPEL, users can leverage additional key metrics such as turnaround timing, study opportunities, and overall study performance reports—enabling you to quickly identify and address bottlenecks to boost startup efficiency and trial performance. PROPEL includes custom dashboards and reports to easily see and share real-time performance metrics by sponsor, CRO, site, indication, and more.  

3. 360-degree View of Your Clinical Trial Operations 

As opposed to a stand-alone CTMS, PROPEL enable sites to store everything related to ongoing and historical trials all in one place. Now, you can attach documents, emails, call logs, and more to individual study records—saving time and eliminating needless email chains, calls, and meetings. Custom tasks, alerts, and real-time threaded chat conversations facilitate cross-functional communication for both central and remote teams. With PROPEL, teams can improve workflows, freeing staff from repetitive tasks and multiple clunky systems so they can focus on winning new opportunities. 

See a full breakdown of how PROPEL compares to a CTMS. 

Seamless Integrations with Industry-Leading CTMS 

PROPEL works in conjunction with your preferred CTMS to provide reporting and analytics across the entire clinical trial process. Data points entered into either system are automatically synchronized across both platforms—cutting out duplicate data entry, boosting efficiency, and decreasing clinical trial cycle times. And because your data is securely stored in one place, drilling down into study and site-specific data and performance insights is simple. 

But PROPEL’s integrations don’t stop at your CTMS. From contact management to email marketing, our open API gives you the power to integrate the tools your team is already using to be successful. Now you can truly have access to all the data and information you need—all in one place.  

From start to finish, PROPEL speeds up the entire clinical trial process, ultimately allowing your organization to respond to more trials and win more of the right awards.  

Already have a CTMS or looking to get one? PROPEL integrates with top CTMS solutions, including RealTime, CRIO, and Advarra’s Clinical Conductor.  

Devana Solutions 

Devana Solutions is an innovative cloud-based clinical trial software company that supports real-time collaboration between central research operations professionals and decentralized clinicians serving patients in diverse communities. Devana Solutions even bridges the technology access and data divide by seamlessly and securely connecting decentralized researchers to other mission-critical clinical trials systems. 

Let us show you in more detail what Better Data, Better Decisions, Better Outcomes could do for your clinical trial processes. Book a demo with Devana Solutions today to learn about our cloud-based data analytics clinical trial software for the clinical trials industry that integrates seamlessly with CTMS and other key systems to keep success in the crosshairs. 

Announcing LYNK UP, a New Clinical Trial Software Solution from Devana Solutions

Devana Solutions is pleased to announce LYNK UP, a new clinical trial software designed for single and emerging research sites. This new product provides research site operations with powerful data visualization and pipeline management capabilities, improving efficiencies, and empowering them to win more trials. 

Devana Solutions is a category-defining clinical trial software company known for providing best-in-class reporting, data visualizations, and dashboards, empowering users with efficient tools for managing opportunities, study startup, trials, documents, tasks, and contacts. Designed specifically for emerging research organizations, LYNK UP is scaled appropriately and offers practical, easy-to-use features. The new software provides transparency into trial status, outstanding tasks, patient enrollment goals, and performance expectations organization-wide. 

“Given the consolidation of research sites into networks that’s been gathering steam, it’s easy to forget that the single, stand-alone research site or sites embedded in a physician practice group make up most of the estimated 10,000 U.S. investigative sites,” said Barry Lake, Devana’s CEO and Co-Founder. “We have not forgotten these emerging research sites and LYNK UP allows them to save time, increase staff productivity, and grow their research volume with a similar category-defining pipeline management, trial startup automation, and metrics capture and analysis technology that is powering the major Site Networks and Integrated Research Organizations.” 

LYNK UP offers a user-friendly and secure solution, enabling site organizations to optimize their clinical trial process, manage their pipeline, and accelerate study startup workflows through intelligent automation. Tracking, sharing, and analyzing performance data in real-time across all trials enables users to make more informed decisions and increase the likelihood of successful clinical trial outcomes. LYNK UP also makes it easy to generate meaningful reporting and metrics for sponsors and CROs, helping organizations win more trial opportunities. 

A one-stop shop for study startup workflow automation and trial monitoring, LYNK UP is designed for clinical trial professionals who wish to transform, streamline, and enhance their operations and capabilities. 

Devana Solutions 

Devana Solutions is an innovative cloud-based clinical trial software company that supports real-time collaboration between central research operations professionals and decentralized clinicians serving patients in diverse communities. Our platform bridges the technology access and data divide by seamlessly and securely connecting decentralized researchers to other mission-critical clinical trial systems. 

Let us show you in more detail what Better Data, Better Decisions, and Better Outcomes could do for your clinical trial processes. Book a demo with Devana Solutions today to learn about our cloud-based data analytics clinical trial software for the clinical trials industry that integrates seamlessly with CTMS and other key systems to keep success in the crosshairs. 

Devana Solutions Welcomes Deb Bawcom as Executive Vice President, Program Management

Devana Solutions is pleased to welcome Deb Bawcom as Executive Vice President, Program Management.

Deb is an accomplished, client-focused software executive with a proven track record of creating high-performing teams from the bottom up with a strong productive culture. She brings years of experience managing end-to-end product and program lifecycles, from innovation to design and delivery, through growth and scale-up phases. Deb has a reputation for successfully guiding challenging change initiatives and for building trusting, lasting connections with customers and colleagues.

Deb joins Devana Solutions with over 25 years of experience in project and risk management in the software, construction, and energy commodities industries. As Executive Vice President, Program Management, Deb will oversee Devana’s product strategy and development, managing product lifecycles and mapping out new features and projects. She will also lead our Product and Solutions Services teams, providing guidance and helping us retain top talent.

“Deb Bawcom’s depth of knowledge in Product Development strategy and, most importantly, execution is a perfect fit for the growth stage Devana Solutions has reached very quickly,” commented Barry Lake, Devana Solutions CEO. “Deb’s skills are going to be critical as we remain on the leading edge of clinical trials industry SaaS innovation.”

Devana Solutions is excited to have Deb join our growing team! With her experience and leadership, we plan to take our product strategy to the next level.

2022 SCRS Site Solutions Summit: The Power of Clinical Trial Software

The 2022 SCRS Site Solutions Summit is nearly here! A big topic this year will be how the industry can continue to extend the reach of clinical trials to new patients and markets. Our continued sponsorship of this event reflects our commitment to improving site solutions through new products and services both now and in the future. 

Join us at Booth 507 for a demo of our transformative software and don’t forget to join us for these other site-focused discussions as well! 

Bringing Clinical Trials to More Patients 

We first want to extend an invitation to Master Workshop III: Innovative Site Models to Bring Clinical Trials to Patients in their Communities on Friday, October 7 at 2:00pm: 

The COVID-19 pandemic and the urgent push for vaccine development and deployment across the U.S. and globally demanded a paradigm shift in how the public and private sectors worked together in Operation Warp Speed to develop effective vaccines in a compressed timeframe. In addition, gaps in access to healthcare and clinical trials across the diverse U.S. landscape required a fundamental rethinking of existing healthcare and clinical trial delivery models.  

Jennifer Byrne, CEO and Founder of Javara,and Josh Rose, VP, Head of Clinical Trial Delivery and Strategy of CVS Health Clinical Trial Services, are leaders of two organizations that were at the forefront of pioneering new delivery models during the pandemic’s most turbulent period. They will be joined by Clare Grace, Chief Patient Officer, of leading global CRO, Parexel, to form an all-star panel to explore how they are now strategically leading initiatives including a Community Alliance Network to address delivering access to clinical trials-as-a-care-option to a wider and more diverse array of patients in the communities at the point-of-care where they access healthcare. The workshop panel will be moderated by Barry Lake, CEO & Co-Founder of Devana Solutions, a leading provider of cloud technology to connect clinical research professionals to clinicians and patients in their communities.       

Win More Trial Opportunities 

Want to be a more competitive site and win more trial opportunities? Be sure to attend Breakout Session III: How to Best Represent Your Site to Sponsors & CROs with Technology on Saturday, October 8 at 4:30pm and learn from industry expert panelists as they share the pro tips and metrics that will have sponsors and CROs looking at your site for more studies.  

Similar to a focus group, this session will be facilitated by FOMAT Medical Research CEO, Nicholas Focil. Featured panelists include Devana Solutions CEO & Co-Founder Barry Lake, Donna Kostandy, Director, Alliance Unit, PPD, part of Thermo Fisher Scientific, Stacie Merritt, Director, Ascension St. John, Al Pacino II, President, HealthCarePoint, and Jean-Marc Tellier, Head, Office of Global Site Partnership, Sanofi 

Devana Solutions 

Devana Solutions is an innovative cloud-based clinical trial software company that supports real-time collaboration between central research operations professionals and decentralized clinicians serving patients in diverse communities. Our platform bridges the technology access and data divide by seamlessly and securely connecting decentralized researchers to other mission-critical clinical trial systems. 

Let us show you in more detail what Better Data, Better Decisions, and Better Outcomes could do for your clinical trial processes. Book a demo with Devana Solutions today to learn about our cloud-based data analytics clinical trial software for the clinical trials industry that integrates seamlessly with CTMS and other key systems to keep success in the crosshairs. 

2022 SCRS Site Solutions Summit: Clinical Trial Data Management Demo

The SCRS Global Site Solutions Summit is just around the corner. Like many others in the clinical trial industry, Devana Solutions is excited to meet with everyone again face-to-face in Hollywood, Florida. There’s something for everyone at the Summit, from top-notch workshops and panels to the many networking events.  

While you’re at the conference, make time to explore the exhibit hall and stop by Booth 507 for a demo of our clinical trial software. Let us show you how we make study startup stress free! 

Meet Our Team

Several Devana Solutions team members will be in attendance, including our CEO & Co-Founder Barry Lake, Vice President of Operations Linda Parks, Executive Director of Strategic Partnerships Michael Bonavilla, Head of Product Alex Schneider, Director of Solutions Services Roxanne Shenefield, Director of Customer Success Bridget Walsh, and Customer Success Manager Zach Denison. 

Come say hi and tell us what you think of our products. We’d love to meet you! 

Let Us Be Your Guide to Stress-Free Study Startup 

Driven by the core belief that performance data transparency through technology is critical to the selection of top-performing research sites, Devana Solutions developed our technology specifically for the clinical trial industry. From pre-award through trial completion, our platform lets you effortlessly manage all of the data and communications along the way.  

Accelerate study startup by having instant access to all the necessary data required. Duplicate data entry, missing or inaccurate information will become a thing of the past! With Devana, organizations can quickly ramp up and enjoy: 

  • Connecting Decentralized Teams 
  • Strategic Site Selection 
  • Digitized Workflows 
  • Multi-team Startup Collaboration 

 And did we mention that Devana Solutions’ cloud-based data analytics software integrates seamlessly with your CTMS and other key systems? Keep success in the crosshairs with quick and easy integrations and other custom solutions for your organization.  

 Want to learn more? Visit booth 507 for an eye-opening demo of our products. During the demo, we encourage you to ask questions about your own requirements and long-term objectives so we can demonstrate how our technology can bring your vision and goals to life. By providing complete visibility into all aspects of the clinical trial process, Devana Solutions can help your research organization streamline processes, automate workflow, and ultimately gain a competitive advantage.  

Devana Solutions 

Devana Solutions is an innovative cloud-based clinical trial software company that supports real-time collaboration between central research operations professionals and decentralized clinicians serving patients in diverse communities. Our platform bridges the technology access and data divide by seamlessly and securely connecting decentralized researchers to other mission-critical clinical trial systems. 

Let us show you in more detail what Better Data, Better Decisions, and Better Outcomes could do for your clinical trial processes. Book a demo with Devana Solutions today to learn about our cloud-based data analytics clinical trial software for the clinical trials industry that integrates seamlessly with CTMS and other key systems to keep success in the crosshairs. 

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