OmniComm offers a comprehensive suite of e-Clinical products and services to meet the demanding needs of our customers.  However, OmniComm recognizes that there are dozens of e-Clinical solutions, both best-of-breed and niche products, that are part of the IT infrastructure necessary to support clinical research.  Therefore, OmniComm has chosen a strategy to support this IT complexity by partnering with select organizations that share OmniComm’s vision and innovative spirit and by integrating shared technologies to facilitate the data management process.  Through these alliances, OmniComm and its partners are better able to solve the complex challenges that our customers face each day as they bring life-saving drugs and devices to market. For more information on the following companies, please click on their logos below.



Algorics brings together a team of highly experienced software and life sciences professionals, united behind a single goal: to provide innovative clinical analytics solutions and software to the global life sciences industry with consistent and reliable quality.  Algorics have designed Acuity a powerful and flexible data aggregation, visualization and analytics platform to provide a clear vision of clinical and operational data and to drive actionable knowledge in real time.  Through efficient integration of data, users can mine retrospective events, monitor real time activity and predict future performance. Customers have used Acuity to gain advantages in many areas including risk-based monitoring, managing operational performance and visually exploring clinical data in real time.


Bio-Optronics is an industry-leading provider of software and services to healthcare and life sciences organizations around the world, and the creators of Clinical Conductor CTMS.  Clinical Conductor is the industry’s first collaborative and configurable CTMS for organizations managing or executing clinical trials. Clinical Conductor provides users with the specific features and functionality they need to effectively collaborate with or among sites and other partners, generate in-depth trial data and reports and maximize profitability. Used by organizations around the world, Clinical Conductor provides organizations with the tools they need to continue to raise the bar in clinical research.


Incorporated in 1998, Clinquest is a Healthcare Product Development Service provider specializing in:

  • Pharmacovigilance Services for Investigational and Marketed Products
  • Medical Information
  • Drug Development Consulting
  • Clinical Trial Implementation
  • Data Management and Biostatistics
  • RT (IVRS/IWRS) for screening, randomization, visit registration and drug supply management

Through our in-house teams and alliances in the US and Europe, we can rapidly assemble virtual pharma teams or integrate into client project teams, providing oversight and expertise to support your individual needs.


Cluepoints is a Central Statistical Monitoring solution that employs unique statistical algorithms to determine the quality, accuracy and integrity of clinical trial data. Aligned with guidance from the FDA and EMA, CluePoints is deployed to support traditional on-site monitoring and can be implemented as the engine to drive a risk-based monitoring strategy.


The cosine team consists of 20 R&D specialists, mostly PhD physicists and engineers. cosine was founded in 1998 and is located in Leiden. A small company full of brain power.

By thinking of new, clever ways to solve problems, the cosine team has regularly come up with original and highly efficient solutions to a large variety of problems. We use our knowledge in physics, electronics and software to solve problems in an innovative way, rather than with incremental steps.

cosine has successfully been involved in finding innovative solutions for technological problems ranging from aerospace technology in service of the European Space Agency to inspection systems for the food industry.


CTIS is dedicated to helping patients around the world by decreasing the amount of time and resources needed for safer drugs to gain regulatory approval. Founded in 1988, CTIS’ information systems have enabled more effective clinical trials research and management by delivering accurate, relevant information to the right people at the right time to facilitate better medical decisions.


Formedix clinical trial automation software and services enable you to remove manual, expensive, inefficient and labor intensive tasks from study set-up, EDC build, validation and submission publication processes.

In fact, across every area of your end-to-end clinical trial, the time and cost savings they deliver speak for themselves and continue to do so time and time again... Formedix saves 68% in set-up time and 55% in EDC build time. With 70% reuse of your content, resources are cut by 23%. It’s all in the numbers.

Your Clinical Trials Automated. Everywhere.



iEllipse Technologies specializes in study implementation across all the leading EDC platforms. With our vast experience in EDC platforms, we are well positioned to guide you on the most suitable platform fitting your needs, based on phase of the study, type of study, therapeutic area, features, help desk support and licensing cost. 

Key Services:

  • CRF Design From Protocol
  • Study Build & Setup
  • Integrations Development
  • Custom Reports Setup
  • Study Validation
  • EDC User Qualification
  • Data Migration


IVR Clinical Concepts is dedicated to developing Interactive Voice and Web Response systems for clinical applications that seamlessly interface with other data collection technologies.

  • Bring your own device. We offer accessibility via telephone, mobile phones, tablets and smartphones.
  • We are ePRO experts and can improve patient compliance
  • No additional hardware costs save our clients money
  • We’re responsive with quick and accurate replies to RFP requests
  • Our clients communicate directly with experienced programmers and expert staff
  • We offer excellent support and provide 24/7/365 availability to sponsors, coordinators and trial participants
  • The staff at IVRCC bring years of clinical trial expertise to your Phase I-Phase IV trials 



Integrated Clinical Systems - developers of Integrated Review™ and JReview® the fastest and easiest way to review, graph, visualize, report, analyze, do patient profiles and patient narratives and Risk Based Monitoring for your clinical data.

Logo Kayentis RVB.jpg

Kayentis is a global provider of electronic Clinical Outcome Assessment (eCOA) solutions for patient data collection in clinical trials. Created in 2003, Kayentis has specialized in eCOA solutions since 2009, developing a full range of services and extending its solutions portfolio to support pharmaceutical companies, biotechnology companies, and CROs. Today, with experience of more than 150 clinical trials in 75+ countries (6,500 sites and 50,000 patients) and in a broad range of therapeutic areas, Kayentis adds value to data quality and clinical trial efficiency with innovative and intuitive solutions.



LogiXML, the leader in interactive, Web-based Business Intelligence, empowers enterprises to turn data into business critical information with its pure Web-based reporting and analysis products. The Company offers a comprehensive platform that addresses all key areas of BI - managed reporting, ad hoc reporting, analysis, and data services. Used by thousands of organizations worldwide, LogiXML products are built on standards-based technologies for easy integration, implementation and upgrade. LogiXMLs per server pricing model makes its powerful technology the most affordable BI solution on the market. Founded in 2000, LogiXML is privately held and based in McLean, Virginia.


Founded in 1982, Mortara Instrument’s headquarters are located in Milwaukee, Wisconsin with European operations based in Bologna, Italy. Mortara Instrument is distinguished in the field of non-invasive cardiology for innovations that are the core of the company’s complete line of ECG products including electrocardiographs, stress exercise systems, Holter systems, data warehousing solutions and cardiology monitoring systems. Mortara products can be found in clinical research applications and healthcare environments worldwide. The Mortara clinical research platform provides investigators, central laboratories and sponsors with a unique set of solutions designed specifically for the workflow of clinical research.

Mosio is a two-way text messaging company specializing in mobile solutions for clinical research. Our award winning Patient Engagement Platform enables researchers to engage and retain study participants through text message alerts, reminders, surveys and interactive “TextChat” features.


pharmaSOL is a leading global provider of innovative technology solutions and expert consulting services for the Life Sciences industry. With a focus on data management, pharmacovigilance and data warehousing, pharmaSOL has been providing high quality capabilities to their pharmaceutical, biotechnology, Clinical Research Organization (CRO) and regulatory partners for over 13 years and have offices in both Europe and the US. Their commitment to delivering comprehensive services including SaaS/hosting, accelerated implementations (rapidLIVE) and innovative applications, allows clients to focus more successfully, and with peace of mind, on their core business needs.


PHT is the market-leading provider of electronic patient reported outcome (ePRO) solutions used in more than 275 clinical trials around the world. Our proven LogPad® and StudyPad® Systems deliver the voice of the patient – directly and without distortion – with reliable and timely self-reported data. By capturing more and better PRO data with reduced variance, sponsors are able to conduct smaller, faster clinical trials. Meanwhile, StudyWorks™ helps sites improve trial management efficiencies with real-time access to symptom, compliance and enrollment data.



Suvoda’s sole focus is to offer the industry’s leading SaaS solution for randomization and trial supply management. Suvoda’s Interactive Response Technology (IRT/IWRS) with Trial Intelligence combines the flexibility of a custom solution with the speed of a configurable platform, offering 4-week deployment timelines, reimagined reporting, and easy integration.


Founded in 2010, Techsol Corporation is a leading global technology service organization, providing pharmaceutical industry focused services in the areas of Medical Information, Drug Safety, Signal Detection and Management, Clinical Development and Pharmaceutical Sales Management. Techsol’ global pharmaceutical – information technology focus and techno-functional expertise enables it to provide technology services and consultancy across the drug life cycle paradigm.   

Partnering with pharmaceutical companies, Techsol helps them adopt digital technology to achieve patient safety and regulatory compliance. Techsol enables them to reach their goals faster and in a significantly cost effective way through its consulting and technology expertise. With over 5 years of experience and more than 40 clients across the globe, Techsol has the ability and intellectual capability to deliver large and small projects with finesse and enthusiasm. Techsol’ flat organization and ‘can do’ culture delivers swift responses, optimal process and faster results.



TRI was founded on the foundation of 13 years consulting experience exclusively dedicated to the life sciences industry. Within this industry, TRI holds a number of “firsts”. TRI is the first and currently the only company entirely focused on risk-based monitoring and clinical quality oversight. They are the first company to create and offer a purpose-built RBM platform, termed “OPRA”. To accompany the OPRA technology, TRI is the first company to approach RBM in a truly holistic manner, providing a full-solution to any CRO or pharma company wishing to implement risk-based monitoring. Specifically, TRI offers the knowledge, services and overall expertise to address the change, processes and management required when implementing a RBM solution. TRI – Where’s The Risk?


Veracity Logic, LLC provides Interactive Response Technology (IRT) systems supporting clinical trials for the Pharmaceutical, Biotech, and Medical Device industries.  Our VLIRT® CORE is an innovative, fully configurable, and customizable IRT system designed to meet your clinical study requirements. The VLIRT® CORE is a validated, 21 CFR Part 11 compliant system that includes Subject and Materials Management, Site and Role based Data Access, Alerts and Messages, with ON-Demand and Scheduled Data Exports.

Veracity Logic, LLC offers the following services to assist you with your clinical studies:

• Customized IWR/IVR system development and validation
• Integration of IWR/IVR data with your CTMS, EDC and/or ePRO systems
• On-going Project Management and Help Desk support

 Contact us at for more information.


Wipro Ltd. is a leading global information technology, consulting and outsourcing company serving more than 900 clients in 54 countries. Wipro helps customers to do business better leveraging our industry-wide experience, deep technology expertise, comprehensive portfolio of services and a vertically aligned business model. Our 55 dedicated emerging technologies "Centers of Excellence" enable us to harness the latest technology for delivering business capability to our clients. Wipro is globally recognized for its innovative approach towards delivering business value and its commitment to sustainability. Wipro champions optimized utilization of natural resources, capital and talent. Today we are a trusted partner of choice for global businesses looking to 'differentiate at the front' and 'standardize at the core' through technology interventions. Wipro is Partner to 4 of the top 5 global pharmaceutical companies, has delivered over 1100 projects to date and has over 4000 associates.

  • Bring your own device. We offer accessibility via telephone, mobile phones, tablets and smartphones.
  • We are ePRO experts and can improve patient compliance
  • No additional hardware costs save our clients money
  • We’re responsive with quick and accurate replies to RFP requests
  • Our clients communicate directly with experienced programmers and expert staff
  • We offer excellent support and provide 24/7/365 availability to sponsors, coordinators and trial participants
  • The staff atIVRCC bring years of clinical trial expertise to your Phase I-Phase IV trials