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Product Registration & Submission Management (RIM)

Provide more controlled and efficient regulatory processes.

Regulatory Registration & Submission Management systems, also known as Regulatory Information Management (RIM), are used to manage life cycle processes of drug development and commercialization. Organizations must effectively and efficiently develop and manage new and existing product information and registration in front of health and regulatory authorities before, during, and after new drug approval.

To achieve this, implement a RIM solution that will rapidly provide your organization with visibility and awareness across your product development life cycles.

Features at a glance:
  • Manage and establish transparency for multiple levels of registration dossiers at the global, regional, and local levels across multiple regulatory jurisdictions
  • Automate processes to allow for simplified data entry
  • Speed product to market with streamlined workflows and a unified interface