Top Crucial Data Solutions, Inc. Alternatives, Competitors & Similar Software

Clinical Trial Management Systems

iRIS, by iMedRIS Data Corporation, is world-class software for pre-clinical and clinical trials, integrating trial functions into an easy to use Web-based application. iRIS modules configure to the specific needs of institutions, creating client-focused programs that eliminate redundancy of data input while maximizing the productivity of trials and reporting. Essentially, iRIS is a suite of tools that assists with the management of time-consuming regulatory requirements. Significantly with iRIS, researchers find that their focus is not on managing essential reporting issues, formerly performed all in hard copy, but on their studies and subjects. Clients receive the most control of any system available, along with both Web-based and onsite training. For over a decade, iMedRIS, based in Southern California, has provided research facilities and institutions with a variety of iRIS modules. Backed by a dedicated team of developers, project managers, and customer support representatives, iMedRIS remains the conscientious forerunner of medical research software design and implementation. All current trends point to completely paperless clinical trial reporting with more research institutions realizing the need for electronic recording methods. The mission at iMedRIS is to provide each client with an integrated management tool with several options to better support each institution’s configuration requirements and needs. With the knowledge and support of the development team and management staff, iMedRIS strives to ensure each client is given the appropriate instruments for a seamless transition to a completely paperless research environment.

Clinical Trial Management Systems

iRIS, by iMedRIS Data Corporation, is world-class software for pre-clinical and clinical trials, integrating trial functions into an easy to use Web-based application. iRIS modules configure to the specific needs of institutions, creating client-focused programs that eliminate redundancy of data input while maximizing the productivity of trials and reporting. Essentially, iRIS is a suite of tools that assists with the management of time-consuming regulatory requirements. Significantly with iRIS, researchers find that their focus is not on managing essential reporting issues, formerly performed all in hard copy, but on their studies and subjects. Clients receive the most control of any system available, along with both Web-based and onsite training. For over a decade, iMedRIS, based in Southern California, has provided research facilities and institutions with a variety of iRIS modules. Backed by a dedicated team of developers, project managers, and customer support representatives, iMedRIS remains the conscientious forerunner of medical research software design and implementation. All current trends point to completely paperless clinical trial reporting with more research institutions realizing the need for electronic recording methods. The mission at iMedRIS is to provide each client with an integrated management tool with several options to better support each institution’s configuration requirements and needs. With the knowledge and support of the development team and management staff, iMedRIS strives to ensure each client is given the appropriate instruments for a seamless transition to a completely paperless research environment.

Clinical Trial Management Systems

MedaSystems’ cloud-based software platform revolutionizes how life sciences companies manage requests for investigational medicines. Our solution addresses critical industry needs by providing automated workflows, collection of real-world data (RWD), collaboration between manufacturers and Health Care Providers (HCPs), and compliance with regulatory requirements in a single, validated platform. MedaSystems offers an all-encompassing solution for expanded access programs, post-trial access, and investigator-initiated studies.

Clinical Trial Management Systems

Discover CISYS LifeSciences' latest solutions designed for your clinical research teams. Our innovative suite of tools, including WebEAS, WebCode, WebFXP, and WebFormX, and WebFXP, ensures seamless operations for clinical research organizations. Established in 1990, CISYS LifeSciences is a global leader in providing eClinical Solutions and Services for the Clinical Research Community. Our technology and services are geared towards reducing costs and timelines associated with clinical trials. Through collaborative partnerships with research organizations of all sizes, we enhance solution efficiencies while minimizing costs. At CISYS, we believe in fostering true partnerships where organizations collaborate to achieve common goals. Our suite of eClinical Solutions supports all phases of clinical trials and is available globally in both SaaS and hosted models. Our Sequence Platform offers modules that can seamlessly integrate or operate as standalone applications. Our Sequence Platform includes: Clinical Event/Endpoint Adjudication (WebEAS) MedDRA and WHO Drug Coding (WebCode) Site Portal/Secure Document Exchange (WebFXP) Patient Eligibility/Enrollment (WebPatient) Smart Forms (WebFormX) In collaboration with our strategic partner, 3D Communications, we are proud supporters of Get Stuff Done 4 Kids (gsd4kids.org), a nonprofit organization dedicated to making a positive impact on the lives of children facing challenges. At GSD4KIDS, our mission is to provide hope, joy, resources, and assistance to these children and their families, demonstrating that they are not alone in their struggles.

Clinical Trial Management Systems

Discover CISYS LifeSciences' latest solutions designed for your clinical research teams. Our innovative suite of tools, including WebEAS, WebCode, WebFXP, and WebFormX, and WebFXP, ensures seamless operations for clinical research organizations. Established in 1990, CISYS LifeSciences is a global leader in providing eClinical Solutions and Services for the Clinical Research Community. Our technology and services are geared towards reducing costs and timelines associated with clinical trials. Through collaborative partnerships with research organizations of all sizes, we enhance solution efficiencies while minimizing costs. At CISYS, we believe in fostering true partnerships where organizations collaborate to achieve common goals. Our suite of eClinical Solutions supports all phases of clinical trials and is available globally in both SaaS and hosted models. Our Sequence Platform offers modules that can seamlessly integrate or operate as standalone applications. Our Sequence Platform includes: Clinical Event/Endpoint Adjudication (WebEAS) MedDRA and WHO Drug Coding (WebCode) Site Portal/Secure Document Exchange (WebFXP) Patient Eligibility/Enrollment (WebPatient) Smart Forms (WebFormX) In collaboration with our strategic partner, 3D Communications, we are proud supporters of Get Stuff Done 4 Kids (gsd4kids.org), a nonprofit organization dedicated to making a positive impact on the lives of children facing challenges. At GSD4KIDS, our mission is to provide hope, joy, resources, and assistance to these children and their families, demonstrating that they are not alone in their struggles.

Clinical Trial Management Systems

InnovoCommerce is the leading provider of AI-augmented study management and site engagement. As the number of clinical trials escalate, global biopharmaceutical companies and CROs are turning to InnovoCommerce's Innovo AI assistant and StudyCloud platform for increased study efficiency and site visibility. Sponsors, study teams, and sites in over 60 countries are enjoying a significant reduction in costs, trial timelines, and burden on their staff by utilizing our eClinical AI copilot and critical site collaboration tools. Learn more at www.innovocommerce.com or email us at [email protected].

Clinical Trial Management Systems

Research Grid (R.grid) is an automation engine for admin-free clinical trials. Our mission is to enable faster, more successful clinical trials by engineering smart software that safely automates back-office admin across the full trial life cycle. Informed by deep expertise and first-hand experience, we have built comprehensive solutions for patient and community engagement (Inclusive) and clinical trial management (TrialEngine) that support a variety of trial types and therapeutic areas. More about TrialEngine: https://www.trialengine.ai/ More about Inclusive: https://inclusive.health/

Clinical Trial Management Systems

Dacima offers an electronic data capture (EDC) and clinical data management software for clinical trials and other research studies with surveys, ePRO, AEFI, patient registry, patient diaries, EMR, and more! Variety of services for database development, data management to web randomization. Customer-focused professional services and support to ensure your studies are deployed quickly and managed effectively. Our staff have extensive industry experience and training materials to ensure your studies run smoothly. To learn more visit our web page at http://www.dacimasoftware.com/

Clinical Trial Management Systems

Dacima offers an electronic data capture (EDC) and clinical data management software for clinical trials and other research studies with surveys, ePRO, AEFI, patient registry, patient diaries, EMR, and more! Variety of services for database development, data management to web randomization. Customer-focused professional services and support to ensure your studies are deployed quickly and managed effectively. Our staff have extensive industry experience and training materials to ensure your studies run smoothly. To learn more visit our web page at http://www.dacimasoftware.com/

Clinical Trial Management Systems

PHARMASEAL was founded in 2016 by a team of industry leaders who share a vision to create smarter technologies and innovative products for the improvement of human health. The company’s first product Engility CTMS simplifies the management and control of clinical trials for biopharmaceutical and medical device companies. Engility CTMS utilises advanced engineering offering enterprise management with rapid deployment, an intuitive user interface and interoperability with other eClinical applications to optimise trial governance and oversight.

Clinical Trial Management Systems

Agents for Accelerated Clinical Trial Design

Clinical Trial Management Systems

Clincase is an end-to-end EDC and clinical data management system providing a complete and integrated environment for the implementation, testing, and conduct of clinical trials for CROs, biopharmaceutical, and medical device corporations. It provides a comprehensive range of features and functionalities while seamlessly integrating ePRO questionnaires to streamline the collection and management of clinical trial data. Clincase keeps data managers, monitors, and sponsors connected to study performance and progress while encouraging increased study participants and site involvement. Clincase has almost 20 years of experience with EDC software. Our team has high expertise in Data-Management, Software Development, Clinical Research, Project Management, and Data Privacy. Meet Clincase, Your All-In-One Clinical Software Suite

Clinical Trial Management Systems

Clincase is an end-to-end EDC and clinical data management system providing a complete and integrated environment for the implementation, testing, and conduct of clinical trials for CROs, biopharmaceutical, and medical device corporations. It provides a comprehensive range of features and functionalities while seamlessly integrating ePRO questionnaires to streamline the collection and management of clinical trial data. Clincase keeps data managers, monitors, and sponsors connected to study performance and progress while encouraging increased study participants and site involvement. Clincase has almost 20 years of experience with EDC software. Our team has high expertise in Data-Management, Software Development, Clinical Research, Project Management, and Data Privacy. Meet Clincase, Your All-In-One Clinical Software Suite

Clinical Trial Management Systems

Developer of a mobile clinical trial management software designed to improve access to clinical trial details through the Web and mobile devices. The company's clinical research technology simplifies continuous site engagement including study updates, cohort updates, clarifications, webinars and weekly or monthly updates as well as provides real-time push notifications, e-mail messaging and read confirmations, enabling researchers to have important trial details at their fingertips.

Clinical Trial Management Systems

InSilicoTrials.com is a web-based platform, which provides a user-friendly computational modeling and simulation environment where many integrated easy-to-use in silico tools are readily available. The platform targets primarily users from the medical devices and pharmaceutical sectors. The in silico tools available for medical devices enable computational testing in different biomedical areas like radiology, orthopedics and cardiovascular during product design, development and validation processes. For the pharmaceutical sector, the platform provides access to in silico tools developed at all stages of the drug discovery and development processes and for many different therapeutic areas. The platform further ensures users management, content protection, simulation solvers, a validated environment, IT security, results reporting, pay-per-use licenses, the computational power of cloud machines and cloud storage.

Clinical Trial Management Systems

Healex bridges the gap between clinical research and clinical care with seamless structured clinical data solutions to accelerate and improve clinical research and trial management. Healex develops and licenses SaaS, on-premises enterprise software and web applications for seamless clinical data management designed to help hospitals, research organisations and pharmaceutical companies with speeding up and executing multi-site clinical trials. Healex provides fully integrated platforms for rapid integration of high-quality, real-time structured clinical data across multiple sites facilitating the move to a FHIR based healthcare industry. By supporting international, open medical data standards such as the FHIR data standard, Healex solutions can be seamlessly integrated into existing hospital systems and electronic patient records, making it easier for patients, clinics and health insurance companies to use clinical data in a wide range of applications. Healex software is proven by over 6300 researchers at 340 hospitals and across 3000+ studies.

Clinical Trial Management Systems

Ancora. ai is an AI -driven, digital clinical trial navigation platform connecting cancer patients to clinical trials.

Clinical Trial Management Systems

Cloud Concinnity® is an integrated platform that centralizes, simplifies and automates control of data, communications, process management & reporting, while unlocking the value of big data. Our platform provides the most functional and comprehensive clinical trial oversight software on the market: a single, secure hub where all meetings, documents and processes can be centralized, automated, monitored and generate a complete audit trail. Cloud Concinnity enables developers of new therapies to bring their treatments to market faster, at a lower cost all while reducing risk to Sponsors, Clinical Research Organizations (CROs) and patients.

Clinical Trial Management Systems

We get our clients to optimise their clinical trials processes. Our aim is to simplify the duties associated to these processes and for that reason we offer the simplest way to deal with them. We listen to our clients and learn their needs to provide specific solutions using our EDC platforms. To find out how we do it, and how we could help your organisation, schedule an introductory call with us: https://www.sharecrf.com/demo

Clinical Trial Management Systems

AI-powered Patient Identification for Clinical Trials