Viedoc is a modern and future-proof EDC that allows clinical trial sponsors and study sites to easily and securely collect, validate, transmit and analyze clinical study data. Designed to be as intuitive as possible, Viedoc saves time and frustration from users at every level, allowing clinical trial organizations to have more focus on their own innovation and leadership.
REDCap (Research Electronic Data Capture) is a secure web application for building and managing online surveys and databases.
Research Manager supports researchers and organisations in preparing, executing and administering (clinical) research data. Our expertise is the collection, validation and enrichment of data. With Research Manager, we offer a research platform that allows researchers to have all functionalities and information in one place and to share it with each other. The platform facilitates researchers who want to be prepared for a future where the patient, access to data, and sharing data are key.
cubeCDMS is the cornerstone of CRScube's unified eClinical platform. Featuring an intuitive user interface and a configurable eCRF builder, cubeCDMS increases the trial team's efficiency during both start-up and study execution. cubeCDMS is a cost-efficient solution, aiming to reduce the overall cost of running clinical trials.<br>
Castor's EDC, ePRO, eCOA, Digital Enrollment, eConsent, eSource, and eTMF solutions enable researchers to easily capture and integrate data from any source and decentralize their trials.
State-of-the-art data collection, storage and productivity tool for organisations that need to generate and manage clinical evidence.
Kneat Gx VLMS Solutions: Your Validation, Your Way Kneat Gx VLMS Solutions is a leading software company dedicated to transforming digital validation and compliance management for the life sciences, biotechnology, and pharmaceutical industries. We believe in Your Validation, Your Way, offering a platform that empowers you to manage, automate, and optimize your entire validation lifecycle with unparalleled flexibility and control. Our comprehensive suite streamlines every step, from document creation and execution to review and approval processes. By digitizing traditionally paper-based procedures, Kneat Gx not only enhances regulatory compliance but also significantly boosts operational efficiency. Our solutions are designed to improve data integrity, reduce costs, and ensure unwavering adherence to industry standards and regulations, all while adapting to your unique validation process.
Dot Compliance is the industry’s first AI-powered eQMS, built to get you up and running fast–and to give you the insights to drive quality efficiently. Our solutions are designed to accelerate safe innovation across the life sciences–with ready-to-deploy process coverage and best practices at your fingertips. Dot Compliance is fully compliant with 21 CFR part 11, EU Annex 11, and supports ISO 9001, 13485, 14971, and 27001.
Ideagen Please Review is a proven, cost-effective solution for the document review, redaction and co-authoring process. Enabling document owners to spend less time on chasing contributions, collating feedback and documenting changes. Ultimately accelerating timelines by up to 65% and delivering more time to focus on the quality of the review.