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.
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.
At Arithmos, our mission is to support our clients in embracing digital transformation that allows them to develop therapeutics for patients in a smart, innovative, and cost-efficient manner.
Since Arithmos was founded, we helped numerous pharmaceutical, biotechnology, medical device, universities, and non-profit organisations to carry out their work in an easier and more efficient way thanks to the technology.
Climedo offers a digital health platform for hybrid clinical trials and observational studies. Its easy-to-use, modular and secure solutions for data management include electronic data capture (EDC), ePRO, eCOA, and Telemedicine. This enables pharma and medtech companies to validate their medical innovations more efficiently in the post-market phase and to capture data in decentralized, real-world settings. As a result, they accelerate studies, save costs, and improve data flow and quality, while fostering innovative trial designs. By connecting all stakeholders (industry partners, study sites, physicians and patients) in one cloud-based system, Climedo is revolutionizing clinical research and making trials more accessible and patient centric. Learn more at www.climedo.com.
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.
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.
Datacapt provides an easy-to-use, flexible, and powerful electronic data capture platform (EDC) for on-site, hybrid, or decentralized Clinical Trials. We allow Sponsors, CROs, Sites, and Patients to work together. Our Platform brings simplicity, efficiency, and quality to the collection of clinical data.
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.
Want to design and build clinical trials faster with less effort? Now you can, with our new clinical metadata repository (CMDR) and automation cloud platform, ryze. We’ve automated manual, labor-intensive processes, and given you the tools to standardize study build and integrate 3rd party platforms.
Simply house your standards and study library in the central MDR, then easily find, manage, and reuse content. Even import content from EDCs and e-clinical systems into ryze. You can design studies for leading EDCs – and see exactly how forms look in ryze without having to build your study.
Instantly convert datasets to SDTM, and make submission deliverables with the click of a button. And all effortlessly in line with CDISC standards. ryze is built on CDISC compliant templates, so compliance is enforced throughout study build. Plus, ryze is a cloud-based off-the-shelf suite, so there’s zero install and it’s ready to go when you are!
Lokavant is a clinical intelligence platform that improves the time, cost, and quality of trial planning and execution through data-driven analytics applications. Lokavant’s platform aggregates and integrates real-time data from disparate trial data sources, and powers advanced analytics enabled by its compendium of proprietary trial data. The suite of applications built on the platform allows study teams to proactively plan and manage their studies and surface insights, driving efficiencies in all scientific and operational use cases. To learn more visit www.lokavant.com.
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.
At Medrio, we believe that clinical trial technology shouldn’t be difficult to use. That’s why our full-service eClinical Data Management suite helps streamline your research and unify your solutions so you have more time to focus on your patients, rather than multiple vendors. Since 2005, our flexible technology has evolved alongside our customers to include an integrated suite of EDC, DDC, eConsent, RTSM and ePRO/eCOA solutions that support your teams and sites, while reducing patient burden.
Let our solutions put you back in the driver’s seat with adaptive technology that easily powers mid-study changes and accelerates your trials, without compromising data quality. Or lean on our global team of experts who are available 24/7 to support you where you need it most. We’ve worked alongside Sponsors, CROs, and sites—spanning all therapeutic areas and trial phases—to secure over 770 approvals, because we know it takes a village to achieve a healthier world. Discover the Medrio difference today by visiting us at medrio.com.
Pharma14 is a leading global medicine database platform used by a wide spectrum of life science companies. Our monthly updated platform is used by governmental agencies, pharmaceutical companies, consultants, CMO’s, API manufacturers, wholesalers and pharmacy retail chains. Pharma14’s robust and accurate medicine data, as well as its industry leading drug pricing reimbursement information give its members the tools required to compete in today’s market. Key pricing drivers such as generics, parallel trade, biosimillars, niche markets and more provide unique industry insight.
Pharma14 can help you.
Track and analyze pricing and reimbursement environments.
Find and create your optimal product launch pricing.
Track historical price movement.
Live track first generics entering the market and create future strategy for loss of exclusivity.
Navigate dossier submission landscape.
Enter price negotiations with full information.
Create and track your own IRP (International Reference Price) data.
Seek out niche markets and products.
Track consumption and sale trends.
Pharma14 full highlights:
• 68 full country medicine database. https://www.pharma14.com/StaticPages/Features
• 2,500,000 medicines (Rx and OTC) – full information about each drug including – Ex-factory, Wholesale and retail prices + reimbursed information.
• Active ingredients, ATC code classification, administration routes, strength, trade names, MA holder information, leaflets in PDF format and much more.
• Niche market product locator.
• Market Opportunity Locator business tool. Live track the molecules with the least competition per country.
• Consumption and sales data for USA, EU5, Scandinavia, Baltics, Canada and more.
• Full European parallel import information. EMA and National levels.
• National medicine shortages tracker.
• First approval date and marketing authorizations for all molecules from USA, Europe.
• Standard monthly updates.
• Real manufacturer information.
• Most competitive and affordable
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.
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