DDi invites you to join us at the MedTech Summit 2018 organized by KNect Life Sciences, a unique event dedicated to the European MedTech ecosystem, to be held on 11-15 June 2018 in Brussels, Belgium.
DDi is unveiling ViSU a centralized Regulatory Information Management(RIM) solution specifically developed for Medical Device manufacturing companies to efficiently manage regulatory data, activities, processes, submissions and commitments.
For manufacturers who are international with affiliates and distributors in several countries, having all regulatory related data at one place accurately and maintaining them continuously is of immense help, both from Compliance reasons and for swift business decisions
ViSU specifically focuses on Post Market Regulatory Information Management modules such as
- Unique Device Identification (UDI)
- Medical Device Single Audit Program (MDSAP)
- Control of Product Release and Shipment
- Regulatory Assessment of Product Changes
- Data to Build Regulatory Strategies
- Planning of Regulatory Resources
DDi is a prominent Technology partner to the Life Sciences industry. We provide smarter technology for Clinical Development, Regulatory and Safety domains by providing innovative technology products and solutions for organizations of various sizes. Our customer base includes organizations from global Top 100 life science companies.
Will you be at MedTech Conference? Set up a time to meet with us!