Medidata Rave is a cloud–based clinical data management system used to electronically capture, manage, and report clinical research data. It enables the user to record patient information (ie, visit, lab, and adverse event data) using forms that are customized for each study.
Connect G2 to Claude or ChatGPT for answers grounded in G2's trusted reviews, comparisons, and pricing from real user insights.
MasterControl Inc. produces QMS software solutions which enable regulated companies to get their products to market faster, while reducing overall costs and increasing internal efficiency. MasterControl securely manages a company's critical information throughout the entire product lifecycle.
Egnyte delivers the only modern content platform that is purpose-built for businesses. Egnyte gives IT centralized control and protection over their files, and users fast access to their content, no matter how or where work happens.
Your all-in-one SOP, document control and training solution. Automate the creation, review, approval and management of Policies, Procedures, Work Instructions, Forms and related content.
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.
Vodori is cloud-based promotional review software built exclusively for life sciences.
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.
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.