cubeTMF

cubeTMF

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Stay Inspection Ready! cubeTMF® manages documents in real-time for quality control and oversight. In accordance with FDA's CFR 21 Part 11, we have developed cubeTMF to provide a validated system for a cohesive workflow for a truly paperless clinical trial. cubeTMF® streamlines the workflow and management of documents, images, and other digital content for clinical trials.
CRScubeCRScube provides a comprehensive and cost-effective suite of eClinical solutions to life science organizations globally. We are dedicated to providing the latest eClinical technology that is fast, flexible, and easy-to-use to streamline end-to-end operations for Phase I-IV, medical device, and Investigator-Initiated Trials. CRScube’s solutions were developed with clinical researchers in mind and meeting regulatory requirements. All solutions are developed in-house and can operate independently or as a unified system, and have been deployed and used in more than 3,000 trials across therapeutic areas and Phases. 

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