January 18, 2016, Princeton, New Jersey:pharmaREADY.com is Navitas’ next generation website for its fully integrated, regulatory compliant document management, labeling, and eSubmission publishing solution suite. Highlighted on the site include new features of pharmaREADY along with new regulatory services, providing a complete-up-to-date overview of the full set of offerings from Navitas.

Navitas Life Sciences previously met with many regulatory professionals at the RAPS (Regulatory Affairs Professionals Society) annual meeting and talked with users in the medical device and pharmaceutical/biotech industry about their needs, and uncovered solutions that can fulfil those needs. Launched in 2003, pharmaREADY^™ has been purpose built to serve the needs of small to medium sized Life Science companies including medical device and pharmaceutical ingredient suppliers. pharmaREADY has the lowest total cost of ownership in the industry and is available in the cloud or on premise. Intuitive and easy to use, installation can be achieved in 4-5 days. During implementation our team of expert navigators will provide training and walk you through your first submission; ongoing 24/7 technical support is also provided.

pharmaREADY provides seamless control over the entire regulatory content management lifecycle, from documentation creation through regulatory submissions. The pharmaREADY suite is comprised of modules for document management, eCTD, SPL (Structured Product Labelling,) TRMS (Training Records Management System) and PPM (Paper Publishing Module.)