Anju is a customer-first organization providing adaptable life science solutions for clinical research, medical affairs, and data science. TrialMaster, IRMS MAX, and TA Scan, the company’s flagship products, reduce complexities in the drug and device discovery and commercialization process allowing our customers to enhance the quality of their patients’ lives.

Customer First
Our mission is to always be a customer-first organization, powered by a passionate team, providing best-value life science solutions paired with an excellent customer experience to simplify the complexities of life science information management.

Driving Impactful Results
Anju solutions are used by large, mid-sized, and small pharmaceutical companies, clinical research organizations (CROs), and medical device companies as well as full-service medical marketing, market research, and communications agencies. Our technologies facilitate data flow between our solutions and seamless communication with third-party systems, providing a unique opportunity for our customers to leverage critical information and drive impactful results.

Web: https://www.anjusoftware.com/

Services: Data Management, Software (EDC), Software (other)

The Clinical Informatics Research Unit (CIRU) operates as an applied research and enterprise unit within the Faculty of Medicine at the University of Southampton. We provide clinical research solutions and services across the globe which advance data excellence, data quality, data management and improve research methods. Just some of the countries we work with include the United Kingdom, New Zealand, Canada, Belgium, South Africa and more.

Our Lead products are EDGE, our Research Management Programme and CORE for Clinical On-demand Research.

EDGE is a global clinical research management system which is embedded into the clinical research infrastructure across 80% of England’s NHS regions, as well as prominently across Scotland and Northern Ireland. Overseas, EDGE is utilised in Canada, New Zealand, Belgium, South Africa, and India. The EDGE Programme offers a unique approach to the management and conduct of research through purpose-built software and provides research professionals with fast access to real-time data. EDGE enables users to track and manage studies from start to finish as well as providing complete control and oversight of patient and participant recruitment. EDGE promotes collaboration throughout its software and improves methods of working, ultimately resulting in better patient care and treatments.

CORE covers a range of expert services which include the design, build and running of electronic forms used in clinical trials across the UK and overseas, including countries such as New Zealand, Brazil, Switzerland and Turkey. Not only does CORE create the forms you need, it also offers randomisation, data management and provides you with those all-important study statistics. CORE captures vital data for researchers working both in the academic world and commercial setting.

Web: https://www.the-ciru.com/

Services: Data Management, Statistics, Project Management, Software (EDC), Software (other)

Clinion is a global clinical technology company that offers AI-enabled eClinical solutions. ClinionAI consists of EDC, RTSM, CTMS, eCOA and Document Automation that cover the entire clinical trial lifecycle. Clinion is committed to innovating the future of clinical trials through ClinionAI and empowering its partners to manage trials more efficiently at lesser costs.

Web: https://www.clinion.com

Services: Software (EDC), Software (other)

Collective Minds is transforming medical imaging through a global, collaborative platform. Our cloud-based solutions connect healthcare professionals worldwide, driving faster diagnostics, improving patient outcomes, and advancing clinical research and education.

Our GDPR-compliant solutions ensure data privacy and security. Trusted by leading healthcare institutions in over 30 countries.

Web: https://about.cmrad.com

eClinical Solutions seamlessly orchestrates clinical technology and expertise to help accelerate the clinical development process. We provide a spectrum of customized data management services and solutions including EDC, Data Management, Clinical Reporting, and Data Standardization, as well as an innovative Clinical Data Hub platform, elluminate®, which brings advanced visualization and analytical capabilities. Through experience and innovation we empower life science organizations to manage and proactively make decisions regarding clinical trials and programs.

Formed in 2006, the eClinical Solutions team has many years of experience working in the life sciences industry dedicated to clinical data management and programming. The organization was formed to address specific needs that our Leadership team identified through their firsthand experiences, specifically to provide unique and high quality solutions for efficient collection, standardization, reporting and role based utilization of clinical research data. Through a consultative approach and the mindset realizing that each individual organization has a unique set of goals and objectives, we have been partnering with our customers to maximize the use of one of their most valuable assets, their clinical data.

Web: http://eclinicalsol.com

Services: Data Management, Software (EDC)

i2e leads transformation for the life sciences industry through best-in-class analytics and technology solutions. Our market leading execution capabilities, along with expertise in analytics & AI and domain knowledge, help pharmaceutical companies, biotech, and healthcare organizations make clinical trials faster, smarter and easier.

Web: http://www.i2econsulting.com

Services: Data Management, Statistics, Medical Writing, Monitoring, Project Management, Regulatory, Software (EDC), Software (other), Freelance Data Management, Contract Staffing

Medidata is powering smarter treatments and healthier people through digital solutions to support clinical trials. Celebrating 25 years of ground-breaking technological innovation across more than 35,000 trials and 10 million patients, Medidata offers industry-leading expertise, analytics-powered insights, and the largest patient-level historical clinical trial data set in the world. More than 1 million registered users across approximately 2,300 customers trust Medidata’s seamless, end-to-end platform to improve patient experiences, accelerate clinical breakthroughs, and bring therapies to market faster. A Dassault Systèmes brand (Euronext Paris: FR0014003TT8, DSY.PA), Medidata is headquartered in New York City and has been recognized as a Leader by Everest Group and IDC. Discover more at www.medidata.com and follow us @Medidata.

Web: https://www.medidata.com

Services: Software (EDC), Software (other), Data Collection Devices

Mednet is a healthcare technology company specializing in eClinical solutions designed for the global life sciences community. Mednet’s comprehensive, EDC-centric eClinical platform improves the efficiency of clinical studies of all types and sizes. Beyond electronic data capture (EDC), Mednet’s solution set provides the tools required to build and manage all types of clinical research, while enabling organizations to adapt to evolving demands and requirements. Pharmaceutical, medical device, biotechnology and Contract Research Organizations (CROs) around the world have trusted Mednet for nearly 20 years to deliver the technology innovation, experience and reliability they need for success.

Our platform, iMednet, is a comprehensive, cloud-based, clinical data management system, centered around a robust EDC and built from the ground up with key native modules, including: Randomization, Trial Supply Management, Adjudication, ePRO, Payments, and DICOM Imaging.

Designed to also allow easy integrations, the platform enables research teams to meet the rapidly evolving requirements of clinical research, while supporting a wide range of study types and designs. iMednet is highly flexible and intuitive, enabling users to get studies up and running quickly, while ensuring easy onboarding of the entire research team and clinical trials sites.

Web: https://www.mednetsolutions.com/

Services: Software (EDC), Software (other)

NNIT is a leading provider of IT solutions to life sciences internationally, and to the public and private sectors in Denmark. We focus on high complexity industries and thrive in environments where regulatory demands and complexity are high.

At NNIT, we bring digital transformation to life. You get a team of leading industry subject-matter experts and technology consultants. We develop, implement, and continuously improve sustainable solutions that help to enhance the quality of life around the globe.

NNIT’s unique blend of global domain expertise and technical know-how sets the company apart as a leading provider of data enablement solutions in the life sciences industry. With a strong track record of success across R&D, clinical operations, and data management, NNIT has the experience and knowledge to help organizations optimize their operations and achieve excellence at every stage of the process and to furthermore unlock the full potential of their data to deliver real business outcomes and ultimately improve the lives of patients worldwide.

We do so, by offering a comprehensive portfolio of services that help clinical teams navigate the complex landscape and to work towards raising the bar for Clinical Excellence.

Web: https://www.nnit.com/

Services: Data Management, Project Management, Regulatory, Contract Staffing

Our Mission:
Revolutionising clinical trials with tech-driven platforms that harness real-world data to drive innovation and accelerate the delivery of life-changing treatments to market.

What NWEH does:
NWEH develop cutting-edge, technology-driven platforms that harness real-world data to transform clinical trials. Our solutions streamline the entire trial process—from feasibility assessments and optimised trial design to participant recruitment, decentralised trial delivery, real-time safety monitoring and advanced data feeds.
By integrating real-world insights with innovative digital tools, we enhance trial efficiency, improve participant experiences and empower sponsors with data-driven decision-making.
We help bring treatments to market faster through smarter, safer, and true-to-life™ clinical trials.

Web: https://www.nweh.co.uk

Services: Statistics, Project Management, Regulatory, Software (EDC), Software (other)

At Qlarix, we facilitate the adoption of Risk-Based Quality Management (RBQM) by offering technological solutions developed alongside our clients for the overall light of clinical studies.

We combine research expertise with innovative technology to empower organizations in their journey towards adopting a robust risk management culture.

WiseCLIN, our RIsk-Based Oversihght System, sets the standard for next-generation clinical trial oversight.

www.qlarix.com

Web: http://www.qlarix.com

Services: Project Management, Software (other)

Science4Tech’s mission is to facilitate access to multiple innovations enabled by technology to improve the quality, rigour and a reliable clinical research based on the scientific method, supporting pharmaceutical and biotech companies in the acceleration of drug development to bring much-needed therapies to patients sooner.

Our data-driven solutions aim to improve all stages of clinical trials, under strict scientific rigour and in compliance with the regulatory framework.

Web: https://s4t.health/

Services: Data Management, Statistics, Monitoring, Software (EDC), Software (other), Data Collection Devices

Suvoda is a global clinical trial technology company specializing in complex, life-sustaining studies in therapeutic areas like oncology, central nervous system (CNS), and rare disease. Founded in 2013 by experts in eClinical technologies, Suvoda empowers clinical trial professionals to manage the most urgent moments in the most urgent trials through advanced software solutions delivered on a single platform. Headquartered outside Philadelphia, Suvoda also maintains offices in Portland, OR, Barcelona, Spain, Bucharest and Iasi, Romania, and Tokyo, Japan. The company’s Net Promoter Score (NPS) consistently exceeds the technology industry average, contributing to the company being selected by trial sponsors and CROs to support more than 1,000 trials across 80 countries. To learn more, visit suvoda.com.

Web: https://www.suvoda.com/

Services: Data Management, Software (other)

At TRI, we implement Risk-Based Quality Management (RBQM) to drive better clinical trials, improve patient safety, and be compliant with Good Clinical Practice (GCP).

Deployed on over 450 clinical trials, we understand the challenges of RBQM and how to overcome them. Our industry-leading RBQM platform, OPRA, is built by operational experts to support Risk Assessment, Risk Management, and Central Monitoring – all in one intuitive system.

With two core modules, OPRA-RAM and OPRA-CM, OPRA enables teams to focus on what matters most, prioritize critical risks, and take confident, timely action – all backed by clear, evidence-driven insights.

What sets us apart? Our operational focus. Whether you need expert support or a seamless tech solution, we’re here to help. With real-world clinical trial experience, our RBQM team provides the guidance you need to meet regulatory requirements (ICH E6/E8) and confidently embed RBQM at the heart of your trials.

That’s why leading global players trust TRI. We’re not called The RBQM Experts for nothing.

Web: https://www.tritrials.com/

Services: Data Management, Statistics, Monitoring, Project Management, Regulatory

Managing clinical trial data should be smooth and simple—regardless of the complexity of your study.

Viedoc solves the data challenges of clinical trial professionals by improving how sites, contract research organizations, sponsors, and trial participants share and manage sensitive data.

Viedoc helps clinical researchers, data managers and other clinical research professionals in capturing, managing and presenting clinical trials data in a intuitive, and seamless solution. Viedoc is a full eClinical suite consisting of EDC, ePRO/eCOA, RTSM, eTMF, eISF, Televisits, medical coding, and much more in one fully integrated solution. If you need integrations – easily set up using our API both for data imported into Viedoc (e.g. wearables, lab, imaging), exported from Viedoc to external systems or a bi-directional integration.

No matter how complex your clinical study may be, working with it should be smooth and simple. Viedoc combines an intelligent core with a streamlined interface and powerful tools, providing reliable access to user-relevant information – anytime, anywhere, from any device.
• Clean, straightforward interface
• Realtime metrics and at-a-glance dashboards
• Quick access to data – 24 / 7, 365 days a year

Web: https://www.viedoc.com/

Services: Software (EDC), Software (other)

Merative is a data, analytics and technology partner for the health industry. For nearly five decades, Merative has combined trusted technology and deep industry expertise to help push healthcare forward.

Zelta™ is Merative’s clinical trials solutions business that includes both a clinical data management and acquisition platform (formerly IBM Clinical Development), and consulting, enablement and extension services. We believe there is a better way to solve today’s – and tomorrow’s – complex research challenges, and we are enabling these solutions in Zelta. Zelta lets you take full command of every aspect of your clinical trials and research. We offer a truly unified clinical data management and acquisition platform with customizable modules that can be tailored to the meet the unique needs of your clinical trials. From the simple to the complex – we can support your research needs.

Web: https://www.merative.com/clinical-development

Services: Software (EDC), Software (other)