With Life Sciences companies being forced to compete, innovate, and execute faster than ever before it is imperative that they are supported with the appropriate technology. As we see the regulatory landscape evolving, and requirements becoming ever more complex, costly, and global in their scope we appreciate that delays in submissions and approvals can happen and, subsequently, increase the risk of non-compliance.

We have developed pharmaREADY^® to ensure robust process optimization for First-Time-Right submissions. The platform is a fully integrated, regulatory compliant, and web-based to create, view, and manage your global regulatory submissions and is available on-premise or in the cloud. The product suite offers several modules that can meet global regulatory requirements: 

• Document Management System (DMS)
• electronic Common Technical Document (eCTD)
• Structured Product Labeling (SPL)
• Training Records Management System (TRMS) 

Please complete the form to download our pharmaREADY^® brochure.

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