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Product Registration Management Solution

Manage Global Registrations with Ease

Why Product Registration Management Solution matters?

Whether you are a few products manufacturer or with 1000s of SKUs, regulatory data and tracking are challenging. Whether through your homegrown tools or Excels or QMS or PLM/ERP, effective planning, tracking and managing of registrations info is not easy. With more Health Authorities moving to Digital from the Document world, it’s not an option of “if” but rather “when”.

Med Device companies’ challenges are different and unique compared to BioParma companies. ViSUis focused on MedTech companies.

Registration management solution for medical devices allows product registration tracking to significantly reduce the risk, effort, and cost of managing global submissions. It assists med device manufacturers to manage new and product life cycle activities effectively.

100+ countries regulatory Requirements DB

Leverage built-in regulatory requirements database that provides country-specific requirements in import/export, market authorization, clinical requirements, testing requirements, safety and life cycle management.

Track Product Regulatory Life Cycle

Get your products to market faster and stay compliant by tracking the entire product registration process, providing real-time visibility and flexibility for global regulations. The solution enables you to track submissions by product, country, franchise, status, milestones, and more. See what additional information is needed to get approval by country. Reuse/clone registration records when expanding product registration to other countries and save time.

Stay Compliant

Commitment/Obligations are created automatically based on the country or you can add/update your own. All these are managed with a calendar-driven dashboard and also set up alerts to help you plan better. In addition, all correspondence from HA/NBs can be automatically pushed into ViSU where these are organized by product or country. This minimizes dependence on some team members’ inboxes or retaining info/knowledge in company when people leave.

Future of the life sciences industry depends on the ability to bring the highest quality products to market quickly and cost-effectively. It takes speed and power to transform the life science product lifecycle. With DDi AI and Automation solutions, organizations can digitize their processes faster and manage complex regulatory processes, without limitations.

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