Take Clinical Trial Management to the Next Level with LYNK

As a technology provider that connects central trial operations teams with decentralized site staff and clinicians, our goal at Devana Solutions is to help research organizations speed new therapies to patients by automating clinical trial processes and capturing site metrics for analysis and execution.

You may be familiar with PROPEL, our enterprise-level platform for managing an expansive research organization consisting of owned or affiliated investigative sites or study teams. By leveraging the cloud to connect central research operations professionals with site-based clinicians and staff for real-time, clinical trial collaboration, it provides easy access to all of the information on trials, sites, users, and contacts at your organizational level. Organizations such as Velocity Clinical Research use PROPEL to create cohesive operations and improve efficiency within their organization and accelerate study startup.

What you may not be familiar with, however, is LYNK—the site-facing extension of the PROPEL platform that expands the capabilities to key site-level staff. LYNK takes PROPEL one step further, giving sites even more ways to streamline processes and increase efficiency. LYNK is the sites’ personalized interface that allows them to receive and respond to trial opportunities and quickly and easily complete feasibility assessments.

Manage Clinical Trial Opportunities

The LYNK interface will automatically notify the sites when a new clinical trial opportunity is sent by the central team. The site LYNK user can review the specifics of each trial, determine which investigator is best for the project, and instantly provide information that is necessary to complete the feasibility assessment. LYNK’s investigator profiles store all vital documents for the sites’ investigators, such as medical licenses, CVs, and training certificates. With LYNK, sites won’t need to sift through emails, document folders, or physical files, because all of this necessary information is located in one place.

Simplify Feasibility Questionnaires

Thanks to LYNK, the cumbersome feasibility process is simplified. Available in the LYNK dashboard, sites can view any outstanding feasibility questionnaires, which will auto populate with the previously answered, common information that is also found in their site’s profile, including contact information, on-site equipment and staff, and specific areas of therapeutic experience. Because LYNK stores all of the necessary data in site profiles, sites won’t need to search for the information in documents and spreadsheets—it’s available instantly.

These are just a couple of ways LYNK works seamlessly in conjunction with PROPEL, providing benefits not only to the greater research organization but to the sites, as well. Book a demo with Devana Solutions today to discover what LYNK can do to take your sites’ clinical trial management to the next level.

Clinical Trial Tech Stack: Seamless Connectivity For Your Team

Clinical trials have evolved in recent years. There are now more decentralized clinical trials than ever before, thanks to the adoption of cutting-edge technologies. However, in order for these trials to be successful from the beginning, it is essential to select the right tech stack. This can be daunting, but don’t worry; the team at Devana Solutions, a clinical trial software platform, is here to help! Here are the key considerations when selecting your clinical trial technology.

During the pandemic, the industry accelerated its growing adoption of decentralized clinical trials (DCTs). This allowed sites to expand their reach and diversify their patient selection. This approach offers several advantages over traditional clinical trials, including:

  • Improved patient access to cutting-edge therapies;
  • Increased efficiency and cost savings due to the elimination of centralization costs (such as those associated with data management and monitoring); and,
  • Enhanced study feasibility due to the use of innovative technologies.

For thriving enterprises in the clinical trial space, developing the software needed to process their needs could be cumbersome. Considering that there are multiple steps and phases, from the business development through patient trials, it can be a daunting task sorting through the different frameworks, languages, and integrations to deliver an optimal experience for your clinical trial organization.

Fortunately for your organization, Devana Solutions has developed the right solution with its IGNITE and PROPEL systems. Adding in LYNK as a communication and data exchange conduit can also keep your teams synchronized when using PROPEL.

Like any comprehensive tech stack, here are some of the key benefits of Devana Solutions.

  • User interface
  • Data storage and security
  • Application integrations
  • Monitoring and performance tools.

Let’s take a closer look at each of these considerations.

User interface

When selecting clinical trial management software, it is important to ensure that the user interface is easy to use and intuitive. In addition, a good user interface can help improve the exchange of information and data between the central teams and remote sites. It can take time to adapt to new technology.

Data storage and security

As teams exchange and use information, cloud-based applications are the easiest to use and store critical data. Throughout the clinical trials, it is essential to ensure that data is stored and accessed securely. This means using an encrypted database that can be accessed only by authorized users. It is also important to have a backup plan in case of system failure.

Application integrations

The best software allows for integrations to enhance the user experience. Devana Solutions integrates with many platforms, including Real-Time CTMS and Clinical Research IO (CRIO) Devana Solutions client-partners also have the benefit of connectivity with communication and interactive data visualization platforms like Microsoft Outlook, MailChimp, and Tableau. Other client-partners benefit from working with Devana Solutions because of the custom integrations made by our technology team.

Monitoring and performance tools

In order to ensure the success of your clinical trial operations, it is important to have tools in place for monitoring and performance tracking. This includes both real-time and retrospective monitoring of data, as well as dashboards that provide an overview of study progress.

Now that you know what to consider when selecting a tech stack for your clinical trial management software, let’s take a closer look at Devana Solutions.

Devana Solutions

Devana Solutions is an innovative cloud 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 software for the clinical trials industry that integrates seamlessly with CTMS and other key systems to keep success in the crosshairs.

Data Analytics & Making Decisions for Better Outcomes

At Devana Solutions, our motto is Better Data, Better Decisions, Better Outcomes. But what exactly does that mean to us—and for you? Let’s take a look at how superior data analytics can make a huge impact on the clinical trial industry as a whole—and your organization in particular.

 

Better Data

We believe complete data transparency is absolutely crucial to clinical trial management. Devana’s cloud-based unified platform allows study teams to securely connect remotely and collaborate in real-time—an essential feature in our era of remote work and decentralized or hybrid trials. To optimize execution, you’ll have the ability to standardize and automate study start-up workflows and connect central research operations teams to decentralized clinicians serving patients in diverse community settings. You can even share “up” to CRO and sponsor partners, ensuring everyone has access to the data they need.

One of our key features to generate superior data includes AI-enhanced auto-email capture and attachment, which links relevant information and documentation to each associated trial, streamlining task management and execution follow-through. Devana also captures start-up/timing metrics and enrollment performance data, whether it’s generated on our platform or via API connections to other systems. It can then display this data on the dashboard, providing leadership and study teams with analysis and action items.

 

Better Decisions

We believe data should work for you, giving you the power to make better-informed decisions. Devana’s centralized business intelligence platform provides access for all stakeholders across the entire research footprint. We leverage information from historic and active trial performance by organization, site, and PI/study team/department—across all indications. With digitized trial opportunities, feasibility distribution, collaboration, and more accurate PI/study team selection and trial feasibility, you’ll see more effective feasibility and trial selection. The Devana platform achieves these results through analyses of therapeutic alignment and your organizational, site/study team and investigator capabilities, as well as your bandwidth. And it provides the real-time trial process and enrollment performance insights your leadership needs to correct bottlenecks and improve trial execution overall. 

 

Better Outcomes

We believe that decisions informed by superior data transparency will produce better outcomes for the clinical trial industry and the patients we serve, period. The Devana platform’s pipeline and study start-up automation, along with its inter-organizational trial communication and collaboration capabilities, saves countless hours previously spent on manual data entry and organization—and reduces human error in the process. With process and performance data transparency, you’ll also see improved accountability across functions and between trial stakeholders.

The right data analytics improve the trial process by matching sites and investigators with the clinical trial opportunities that suit them best. When more reliable PIs and study teams are aligned on the right trials with industry sponsors and CROs, you’ll see the results in increasing predictability of trial performance and more trial opportunities. This reduction in trial cycle time and cost means faster delivery of new therapies to patients.

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 software for the clinical trials industry that integrates seamlessly with CTMS and other key systems to keep success in the crosshairs.

 

2022 SCRS Global Oncology Site Solutions Summit: What to Expect

SCRS Oncology Site Solutions Summit

If you work in oncology research, you likely have your eyes set on the upcoming 2022 SCRS Global Oncology Site Solutions Summit. The team at Devana Solutions, is excited for this year’s event. Devana Solutions helps central research operations professionals and decentralized clinicians stay connected and aligned to optimize the entire clinical trial process.  The 2022 Oncology Site Solutions Summit takes place on January 28 and 29 in Austin, Texas.  If you aren’t familiar with an SCRS Site Solutions Summit event, check out our recap from the 2021 SCRS Global Site Solutions Summit.  

The SCRS Oncology Site Solutions Summit takes place at the Hilton Austin, and  offers a chance to those in the oncology research field to connect and innovate.  Here’s a preview of what to expect.  

Network with Industry Leaders

One of the advantages of attending the SCRS Global Oncology Site Solutions Summit is to connect, in person, with oncology research teams and leaders, from the sites to CROs and Sponsors to industry vendors; sharing valuable insights in an effort to advance the mission in finding new treatments and, someday, a cure for cancer. 

Between networking breaks and partner lunches, there are opportunities to connect with longstanding peers or make new professional relationships.

Learn About Innovation in the Field

The interactive discussions truly make the SCRS Global Oncology Site Solutions Summit a must-attend event.  

We are big fans of the breakout sessions. Some of our biggest areas of interest are around making the , improving clinical trial management during study startup and connecting central operations teams with clinicians.  We’ve broken down some of the sessions we are most excited about at the Oncology summit in Austin:

 

Friday, January 28, 2022

11:00 am – 12:00 pm

BREAKOUT SESSION I

Among the topics we are interested in:

  • Protocol Feasibility: Tactics & Tools for Success
  • Hybrid Decentralized Trials: Critical Considerations 
  • Trust-Building: Utilizing Your Data to Validate Your Site

 

1:00 pm – 2:00 pm

BREAKOUT SESSION II

Among the topics we are interested in:

  • Quality Focus: Does Your QMS Need a Refresh?
  • Site Perspective: Managing the Life Cycle of Clinical Trials

 

2:30 pm – 3:30 pm

BREAKOUT SESSION III

Among the topics we are interested in:

  • JIT Applications & Other Assessments: Are They Right for My Site?
  • Understanding & Integrating Electronic Clinical Trial Documentation Systems
  • Site Network Consolidation: What Does it Mean for You?
  • The Impact of Wearables in Oncology Studies

 

Saturday, January 29, 2022

10:30 am – 11:30 am

BREAKOUT SESSION IV

Among the topics we are interested in:

 

  • Site-Centricity & Relationships: The Importance of Site Needs (Option A)
  • Site-Centricity & Relationships: The Importance of Site Needs (Option B)
  • The Best Staffing Models for Better Quality, Enrollment & Margins

 

Grow Your Business at 2022 SCRS Oncology Site Solutions Summit

Through all of the networking and interactive sessions, the most important take-away from attending events like the 2022 SCRS Global Oncology Site Solutions Summit is developing new partnerships that help to carry out our mission to improve clinical trials and speed therapies to patients faster.

Are you planning on attending the 2022 SCRS Oncology Site Solutions Summit?  We’d love to chat. Devana CEO and Co-founder Barry Lake and Director of Strategic Partnerships Emily Hardy are excited to discuss how technology can improve the clinical trials space for oncology and beyond.  Connect with Barry or Emily on LinkedIn or use the contact form at the bottom of the page to set something up before the big event in Austin!

 

 

 

Why Automated Data Analytics are Crucial for Clinical Research Leaders

The sheer volume of data produced by the clinical trial industry is staggering—and it’s growing every day. The healthcare industry, in general, relies on big data to function, and clinical trials are no exception. We need speedy, secure access to data sets that are large, complex, and diverse. By and large, big data has moved onto the cloud in recent years. Yet because of the limitations of the applications and processes used by most clinical research organizations, much of the information remains siloed in different systems. We end up spending hours trying to wrangle data from multiple sources in an effort to get the insights we need to effectively manage operations. But what if the clinical data you need wasn’t just scattered across multiple software systems (and spreadsheets)? What if you had a single platform from which to manage all of the information you need to maximize the efficiency of your research and speed medications and treatments to the market? What if, instead of sifting through disparate systems to gather and analyze pertinent data, you could automatically generate your data analytics with a few clicks? Below are just a few of the opportunities made available through automated data analytics. 

Optimize Clinical Trials

With the ability to analyze trial performance data in real-time, you’ll easily choose the best sites and investigators for your research, track trial progress, make informed decisions, and improve outcomes. With more accurate data, you can improve trial efficiency and lower overall costs.

 

Ensure Accuracy & Improve Data Quality

A streamlined platform that can integrate your systems will improve the accuracy and quality of your data. Manual methods of data gathering are tedious and prone to error. With automated data analytics, it’s much easier to see inconsistencies and gain valuable insights, and you’ll save valuable time.

 

Speed Up Treatment & Drug Development

With access to more historical data and the ability to analyze it automatically, you’ll gain better insight into the potential outcomes of current and future trials. A more efficient trial process also accelerates the pace at which you can develop new medicines and treatments—and get them to the patients who need them. 

These are just a few of the benefits automated data analytics can bring to clinical research leaders. With a cloud-based SaaS that integrates seamlessly with CTMS and other key systems to provide you with automated data analytics in real-time, you’ll get instant access to the insights you need to make better decisions and increase your chances of a successful outcome.

Book a demo with Devana Solutions today to learn more about our cloud-based data analytics software for the clinical trials industry that integrates seamlessly with CTMS and other key systems to keep success in the crosshairs.

 

Transform Your Clinical Trial Processes in 2022

While those of us who work in the clinical trial space have always known that the importance of our work cannot be overstated, there’s no question that the COVID-19 pandemic has driven home the importance of the clinical trials industry to the rest of the world as well. As we reflect back on the events of the past year, Devana Solutions is proud of the role we have played in supporting the development of life-saving vaccines, treatments, medical devices, and medications that have had a positive impact on quality of life for the patients who received them. As we look forward to 2022, we remain dedicated to supporting new discoveries in the field of medical research.

At Devana, we know that clinical trials are an essential part of ensuring that real people get the care they need to live better lives. We’re also aware how limited the options have been for managing clinical trial processes. Labor-intensive manual data entry and scattered spreadsheets with incomplete or missing information are common. Often “the left hand” will have no idea what “the right hand” is doing, especially if both of those “hands” belong to a research organization conducting more than a handful of trials at once. That’s why we developed our technology—to help you bring your goals for the future of medicine into alignment with your capabilities as a site, CRO, or sponsor. 

While there’s no telling what kinds of challenges 2022 might bring; the cumbersome, error-prone processes you currently struggle with don’t have to be among them. Imagine, instead, the opportunities that will unfold with Devana’s clinical trial technology that provides you with a single, cloud-based platform with real-time data.

From pre-award through  trial completion, our platform lets you effortlessly manage all of the information along the way. Clinical trial processes become a snap when you have instant access to all the necessary data required. You won’t have to worry about inaccuracies slowing down the trial award process and startup stage, because all of the necessary data for a site can quickly and easily be assessed and shared with CROs and sponsors. 

As your single solution to standardize, streamline, and automate all of your clinical trial processes, our platform will help you align with the right trials and speed therapies and treatments to the patients who need them most. Let 2022 be the year you take the first step towards transforming your clinical trial processes with Devana Solutions.

Book a demo with Devana Solutions today to learn more about our cloud-based data analytics software for the clinical trials industry that integrates seamlessly with CTMS and other key systems to keep success in the crosshairs.

 

How Technology Simplifies Clinical Trial Feasibility Assessments

Ah, the dreaded site assessment and feasibility: pages upon pages of requests for information. From equipment specifications to investigator experience to patient population, the amount of data needed to execute a clinical trial feasibility is onerous. You may have most of this information on hand—across a variety of spreadsheets, emails, documents—and in your head. But there may also be gaps in the information you have access to, leaving you no option but to put down your best guess and muddle through.

However, the accuracy of the data you provide in an assessment is vital. Sponsors and CROs need the information in a feasibility to be as precise as possible, or else how can they be sure a site will be able to perform as needed in a trial? Miscalculations and incomplete information could prevent you from being awarded the trials you deserve. On the other hand, an inaccurate feasibility could lead to being awarded a trial that your site cannot perform well, resulting in damage to your business and your reputation. This inevitably slows down or even halts the investigational process, causing delays in much-needed therapies, vaccines, and devices making it to the market—and to the patients who would benefit from them.  

Clinical Trial Feasibility Accuracy and Innovation

In the clinical trials industry, innovation and state-of-the-art technology are a part of the job. But until now, so many sites have been relying on outdated, error-prone manual processes to store and deliver their vital information. Devana Solutions is here to change that by bringing site feasibility assessments into the 21st century. With our clinical trial process management platform, you’ll have access to all of the data you need to flawlessly execute clinical trial feasibility assessments—within seconds. 

Performance for Indications & Therapeutic Areas

Devana’s platform gives you the ability to review a site’s past and current performance, as well as their experience in particular indications or therapeutic areas. This information can be displayed for your particular site, for a specific investigator, or even for the organization as a whole. You can easily see the number of trials and average enrollment metrics for those trials, such as patient volume, screen failure rate, early term rate, and contract fulfillment percentage. 

Performance with CROs & Sponsors

Common feasibility questions about your performance with specific CROs and sponsors include queries like how many studies are you currently running or have completed for a specific CRO or sponsor? What is your average study start-up time with that same CRO or sponsor? How long on average does it take your site(s) to screen the first patient once the study has been given the “green light?” Devana’s platform instantly provides this information for you. Among other metrics, you can see the number of trials performed for each CRO and sponsor, their turnaround time, and pertinent enrollment data. 

Clinical Trial Feasibility Investigator Information

Our platform’s investigator profiles centrally house all of the crucial documentation for your investigators, including CVs, medical licensing, and training certificates. No more digging into emails, computer folders, or physical files of photocopies just to fill out the investigator information in a feasibility assessment. With Devana’s platform, everything you need is in one place.

Site Information

All of the relevant information needed for a site feasibility assessment—from the basics such as contact info to the nitty-gritty details like therapeutic area experience, equipment on-site, staff-on site, and past FDA audit outcomes—is stored in our platform’s site profiles. You won’t need to sift through countless documents and spreadsheets just to get the necessary data—our platform provides it at the touch of a button.

Financial Information

Budget considerations are a common element of feasibility assessments, requiring you to provide fiscal details in a variety of areas. This financial information includes costs related to specific indications as well as particular CROs and sponsors. Devana’s platform stores and crunches the numbers for you, so it’s available anytime you need it. 

Feasibility assessments are essential for winning trial awards, but there’s no reason they should still be a stressful, manual, error-prone process. With Devana’s platform, you’ll effortlessly give CROs and sponsors the data and the insights they need to understand your strengths and weaknesses, optimize your performance, and win study awards.

Book a demo with Devana Solutions today to bring your clinical trial feasibility assessments into the 21st century.

 

How to Better Manage Your Clinical Trial Operations

One of the biggest challenges that clinical research organizations face is managing their vast influx of clinical trial opportunities from Sponsors, CROs and other potential sources. As anyone in this industry knows, there’s a lot of effort that goes into starting up a clinical trial; from sourcing the trial, to feasibility and site selection, to contract and budget negotiations, to regulatory and the many steps in between. Even today, in this advanced digital age, most research organizations are still relying upon mundane spreadsheets and manual processes to manage their trial activities. Why are we still doing this when there is technology available to make our lives easier? Devana Solutions’ innovative platforms help to increase efficiency around clinical trial processes for research organizations of all sizes, with varying needs. 

Managing New Clinical Trial Opportunities

Devana Solutions helps you track the pipeline of new clinical trial opportunities.  

Let’s say you’re a research organization with ten site locations that was just approached with a new clinical trial opportunity. In Devana, you can create the trial opportunity, once, completing details such as the name, trial origin, therapeutic area, protocol number, etc.; details that will not change regardless of which sites are conducting the trial.

Once you’ve created the trial within Devana, you can then add all ten sites to the trial, which creates a site activity and enrollment record for each site. Whether startup activities are handled centrally or at the site level, you will be able to track the completion of necessary milestones within Devana. If certain milestones are handled centrally, you only have to update the milestone once from the main trial page instead of having to update each individual site record, 10 different times.

Devana also offers built in, automated task management so important tasks never get missed, since we know there are many moving parts in managing a trial, in all stages.

Simplify Feasibility Questionnaires

One of the more frustrating situations during the feasibility process is not having complete data to quickly and easily respond to feasibility questionnaires.

When you have this information in a comprehensive system like Devana Solutions, it makes responding to a feasibility much easier since everything is at your fingertips.

One area where this is immensely beneficial is having concrete data surrounding your investigators’ historical and current trial performance. When completing feasibilities, do you know, without hesitation, how many trials they’ve participated in? Can you easily tell how many they are actively conducting? Or perhaps the feasibility is asking for data related to the indication. Do you know how many trials you’ve completed in a particular indication? What about your average enrollment percentage in that indication? Or screen failure and patient retention percentages? Devana Solutions allows you to instantly access data whether it’s sorted by the trial, indication, investigator, site or the entire organization.

Sort Your Decentralized Site Data in Seconds

In the age of decentralized trials, it can be difficult to sort through each sites’ capabilities to determine which sites are compatible when presented with a new trial opportunity. Sure, you may have a spreadsheet detailing each sites’ therapeutic capabilities and equipment on site, but how time consuming is it to sort through this information manually? Or what if a site makes a sudden change to their capabilities? How can you be confident that the information you have on hand is accurate? Certainly, you can call or email the site each time you receive a new feasibility, but who has time for that? 

These manual processes may not be too cumbersome if you have two or three sites, but what happens when you have two to three dozen or more?  Devana Solutions tracks all of the key information for each site so that you are able to quickly query the data for all site locations to determine which sites or investigators are capable of conducting a particular trial. But how can Devana help ensure that you always have the most accurate data on your sites? Through Devana’s site-facing interface, LYNK, which allows site-level users to update their capabilities in real-time, so that your teams can be rest assured that the information they rely upon for precise site-selection is accurate.

Is your site maximizing its potential to conduct trials more efficiently and reliably? Are you easily able to access critical data to make better business decisions? If not, you’re not alone. Come join the numerous industry leaders who made the decision to partner with Devana.  Book a demo with our team by clicking here, or fill out the form at the bottom of this page.  

 

Clinical Trial Analytics Visibility Has Never Been Easier with Devana Solutions

Bridging data gaps in the clinical trial space can be the deciding factor in losing and securing clinical trial opportunities. If you’re in the role of business development, you’re likely the one who is most concerned with bridging these gaps, hitting your clinical trial targets, and winning more awards. But do not fret, because once you tap into the power of Devana Solutions, a comprehensive clinical trial analytics platform, business decisions have never been simpler and as precise.

Devana Solutions’ Clinical Trial Analytics Platform Expands Visibility

While you may already have systems in place that provide data on an active trial, you may be operating with blinders that cause you to miss crucial data points for your entire research operation. By utilizing Devana Solutions, you can make more informed decisions by expanding and opening up your peripheral clinical trial vision to analyze real-time data across your entire investigative footprint.

How much visibility do you currently have once you receive a new protocol synopsis for consideration?

Applying Devana Solutions’ Clinical Trial Analytics Platform to Your Protocol Synopsis

Our clients tell us that one thing that hindered them before using Devana Solutions’ clinical trial analytics platform was a lack of visibility into their research operations, as a whole. They share that they value Devana Solutions’ ability to recognize potential for additional opportunities. Instead of hunting for opportunities, one by one, Devana Solutions allows them to filter and collate all of the opportunities into one easy-to-use dashboard that’s customized to what’s important to their organization.

Devana Solutions helps business development decision-makers gain insight into their organization’s potential, including, but not limited to:

  • What resources do we have available to conduct a new trial?
  • What indications do we perform well in (or those we do not)?
  • What is the forecasted revenue for trials in this indication?

View Your Opportunities and Research Operations with Devana Solutions’ Clinical Trial Analytics Platform

Let’s say that you have four active and enrolling trials, in the same indication, that your site(s) is doing well. Because of this success, you’ve been approached to conduct additional trials in the same indication, but you need to determine which is the best fit for your organization or if you have the necessary bandwidth and patient population to conduct. Devana Solutions‘ clinical trial analytics platform presents you with a broader view into these opportunities, as well as your research operations, to help make this decision faster and more accurately.

With real-time data at your fingertips, a cloud-based platform to house your account and contact information and email integration to never lose sight of important interactions, Devana Solutions is the answer to connecting and aligning your site(s) with CROs and Sponsors for more of the right trial awards.

Devana Solutions’ Case Study

Help your organization gain the competitive advantage and narrow the hunt for opportunities, while staying on target. Learn more about what Devana Solutions is doing for Medical University of South Carolina in this case study.

Take a Devana Solutions Demo

Better yet, let us demonstrate the Devana Solutions platform for organization and talk about your specific needs. Click here to book a demo or use the form below.