Clinical trial management solution that helps manage clinical projects, documentation & biostatistics through data coding, CRFs & more.

Designed specifically for the communication needs and compliance requirements of life sciences and research facilities, Path Clinical reduces costs and maximizes efficiency by quickly connecting trial investigators in any location to improve retention and increase compliance.

Replior's TrialOnline is a clinical research platform that enables sponsors and CROs to provide a software-as-a-service, SaaS, solution for study teams to easily consent and enroll participants. Collect data from investigators, patients, or wearables with ease and select if studies will be operated with site visits, remote visits, or as a hybrid model. Trial Online suit includes ePRO, EDC and Virtual, for remote and decentralized trials.

Delve is a cloud based solution providing a search engine allowing users to look at data across multiple streams identifying what they need. The most popular use cases that our clients have used Delve for are: 1. Automating Literature Review. 2. Pre-qualify Investigators and Sites based on the work they have done in regards to Clinical Trials and publications conducted. 3. Gather insights in regards to the different trials conducted, where they happened and so forth.

EasyTrial is an online Clinical Trial Management System for handling and administration of all tasks (operational and logistical) in clinical studies, so healthcare professionals can use their time efficiently. The system has been developed by Danish doctors experienced in conducting clinical trials. EasyTrial is compliant with Good Clinical Practice (GCP) and legislation applicable to database security and it provides maximum security, study overview and resource handling.

Help your Clinical Operations team continuously improve speed, efficiency and data quality across your portfolio of clinical trials

A disruptive big data SaaS platform, that accelerates new drug launches,lowers clinical trial costs, and enables RBM.

21 CFR Part 11 Compliant, Web-Enabled eClinical Suite with integrated Clinical Trial Management.

The "Astracore Clinical Trials System" is a cloud-based solution for your CRF or eCRF needs. Very quick to set up for your specific needs with many features, and readily customizable for any unique or specific features. Able to store supporting documents, images, audio and video. Can upload existing CRFs or data collection templates or start from scratch. Free and non-obligation custom configuration and trial available - just contact us for details.

Whether as a sponsor, CRO or SMO BSI life sciences software covers your specific processes and features. Plan and manage all aspects of your clinical trials like patient engagement, clinical trial management (CTMS), trial master file (eTMF), study start-up, and trial supply management (RTSM) with the clinical software solutions from BSI. Regardless of whether you need a completely new system, or would like to improve your existing CTMS, you are in the right place with BSI.

A powerful Clinical Management System with end to end modules such as appointment scheduling, billing, EMR, and more.

Trials.ai leverages artificial intelligence to manage clinical trials.

Are you tired of using a CTMS that is overcomplicated, has a poor user interface and costs way too much money? At Intrinsic, we solved these problems by developing an easy to use practical CTMS that is cloud based. Intrinsic has 4 key clinical software productsCTMS, eTMF, study portals, and investigator portalsthat help pharma companies more easily manage their trials and CROs. Each module can be purchased separately, or users can enjoy the benefits of an integrated suite of clinical systems.

An interactive environment for multimodal biosignal data processing and analysis in the fields of clinical research and life sciences

KLINDAT is a next-generation electronic Case Report Form (eCRF) for the pharmaceutical, biotech & medical device industries.

A new breed of cloud-based, patient-centric data capture solutions designed to handle both ePRO and EDC on BYOD.

A plataforma de suporte a estudos clínicos da Longboat cria um ambiente no qual a conformidade com o protocolo é instintiva, as equipes estão sob orientação praticamente contínua e todas as partes interessadas têm o conhecimento e os recursos necessários para conduzir o estudo clínico. Equipes de operações clínicas, monitores, equipe do local e pacientes acessam a plataforma de suporte integrada e consistente. A interface e o suporte fornecidos se ajustam para atender às necessidades específicas dependendo da função dos usuários no estudo.

A robust clinical trial management system, providing you powered capabilities with simplicity, enabling further speed of site selection and startup, enrollment, and execution and tracking all while integrating with your other existing systems, to ensure seamless flow of information across your operations. Innovative modern pharmaceuticals often require a deeper understanding of the entire trial life cycle in order to effectively reach the goal of treating and preventing disease.

LINEA System is a leader in helping accelerate clinical trials by leveraging data and automated technology in a completely new way. Our cloud-based Study Start-up Management System (SSMS), AcceleTrial, enables sponsors to streamline and automate the study startup process to drastically reduce the launch time of clinical trials and patient recruitment. When a clinical trial begins faster, critical medicine gets to patients who need it most.

Comprehensive eSource system for all the source data for clinical trials with source, regulation, and drug accountability.

Ready to use clinical trials management platform that helps govern all parts of the research process.

Electronic Data Capture (EDC) system for the collection of trial data in an electronic format for use in clinical trials & RD.

Configurable CTMS that helps clinical operations manage global trials of drugs, devices, biologics, and vaccines in all phases.

Document management system designed for handing documents dealing with clinical trials management.

Inato helps life science companies make effective recruitment decisions based on machine learning and collaborative site selection.

The comprehensive AssessRx solution is designed to assess a clinicians ability to consistently and safely apply clinical knowledge, skills, and judgment through the use of multiple valid and reliable assessments. This solution helps organizations quickly identify a clinician's ability to recognize and respond to urgent patient situations as well as effectively communicate with others within the healthcare team.

Nucleus is a platform that combines all aspects of clinical development into one convenient location, allowing you and your team to manage documents, communicate with one another and access your clinical information from the same application.

Management software for clinical trials including tasks, events, documents, and visits.

Allows data capture from any location to reduce clinical trial time and cost.

Clinion CTMS is the new age Clinical Trial Management system, which allows you to efficiently manage multiple clinical studies and obtain real time information about recruitment across sites, SAE / AE reporting, Budgeting, Expenses and invoicing, Scheduling and monitoring of sites, site reports etc. Clinion-CTMS is flexible, scalable and integrated cloud based web application available as SaaS (Pay as you use) model.

An advanced electronic data capturing and clinical trial solution built specifically for the oncology department.

Cloud-based clinical trial data management solution that comes with integrated randomization models, built-in QA control, data change tracking, and graphical tools.

VirTrial's Virtual Care Management (VCM) platform is a proven telemedicine solution customized to drive adoption of hybrid decentralized clinical trials (DCTs). By combining best of breed technology, an open API for interoperability, and support for hybrid trials, the VirTrial VCM platform is the most flexible solution on the market. The VirTrial VCM operates on any device (Android, Apple, phone, tablet, computer) and works with any clinical research site worldwide.

ABA data collection & graphing software. Programs update automatically based on phase settings, chaining types, and sequential goals.

PhysioQ simplifies the physiological data collection and management process for both researchers and participants. It makes collecting data secure and possible from anywhere. PhysioQ is a nonprofit organization focused on helping the diverse health researcher community to collect and analyze physiological data. From health researchers running exploratory research in their lab to managing clinical trials with hundreds of participants.

We are a recognized, industry leader in the IRT market and eClinical field, and have implemented over 1,500 clinical trials requiring patient randomization, clinical supply distribution and returns/destruction accountability. In over 10 years of operation, Cenduit has worked closely with more than 100 global biopharmaceutical companies and has deep integrations with many CROs, across all geographies.

TRACK HUMAN BEHAVIOR. REDUCE HUMAN ERROR. MicroStudy is the accurate cloud-based data collection solution for clinical research. Now you can use a software system that is intuitively designed, easy to set up and easy to use for simple and complex studies. Our automated system delivers the ability to track data in real time and generate reports on demand. MicroStudy training is customized to your team, and support services are responsive to your needs -- as you need it.

An AI platform that allows clinical trials to predict complications 7 days in advance

Communication tool for accurate and immediate information for clinical trials

Clinical researchers who earn RBQM Essentials certification become key stakeholders in improving the output of clinical operations within their organizations. They strive to optimize data quality and patient safety in clinical trial conduct by implementing risk-based processes and establishing metrics, KRIs, KPIs, and QTLs, that minimize the potential for error, misconduct and fraud. White Belts participate in clinical research and problem-solving tasks related to QM and risk reduction.

cubeCTMS is our integrated clinical trial management system that is packed with convenient features that aid the management process: high-level tracking, monitoring visit report workflows, various dashboards and many more! Furthermore, cubeCTMS is fully integrated with CRScube's EDC solution: cubeCDMS. Resulting in saved subject, SAE PD/PV data being automatically synced. Please contact us for further information and a demonstration of our integrated platform.

BizNET, A clinical trials management software offers an integrated suite of software products for CROs, Pharmaceutical, Biotech Industries and Medical device industries. Our solution blends various integrated modules that prominently support clinical trial activities like EDC/DDC data collection, IWRS & drug randomization management, CDISC SDTM. It is a validated software, compliant with 21 CFR part 11 and GxP guidelines which provide a transparent and smooth process to regulatory

niAnalytics GmbH offers a unique and comprehensive set of software and services solutions for pharmaceutical and medical device companies, sponsors, contract research organizations, as well as academic institutions and hospitals. Our data management approach supports all types of clinical trials and post-marketing studies. Whether you are a pharmaceutical or medical device company, academic or clinical institution, the niAnalyitcs ecosystem will help you succeed.

Clinical research solution that helps you manage clinical trial operations and data, from patient data to financial tracking.

Enables collaborative, web-based, privacy-first data management for clinical research.

Empowers medical researchers with simple yet powerful software that provides high quality, standardized data.

Digital healthcare software able to function without EMR.

Helps streamline document workflows, compliance, and more for clinical trials.

Heavy lifting across the entire research lifecycle. Developed over more than a decade of deep engagement with the research sector, OmniStar Research does the heavy lifting across the entire research lifecycle. By integrating and automating processes from ethics reviews to grants, scholarships to research governance, IP to reporting and so much more, the OmniStar Research management system gives researchers more time to do what they do best make a difference.

For biostatisticians who want to more quickly and easily design efficient clinical trials with favorable operating characteristics, East is a user-friendly system that simplifies application of the most prevalent fixed, complex, innovative, and adaptive clinical trial designs. East, developed by respected thought leaders in clinical trial statistical design, has been trusted around the world for 30 years by industry and regulatory agencies, and continued investment keeps East at the forefront.