Our client, a mid-sized pharmaceutical company researching and developing novel dermatological treatments, were seeking a web-based software solution to meet the immediate needs of both their Quality Assurance and Regulatory Affairs teams. In addition, they needed to add new enhancements and features to accelerate the life cycle of document workflows and submissions in order to deliver faster, with improved accuracy and better efficiencies.

Read our case study and learn how Navitas Life Sciences successfully delivered pharmaREADY^® DMS and eCTD modules to meet our clients needs and to ensure 21 CFR Part 11 compliance. Our client is now benefiting from:

• Paperless Audit Preparedness
• A Centralized Repository for One Source of Truth
• Ability to quickly batch import using the ‘Submission Import’ utility

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