Keep detailed notes on communication, upload documents, and track important dates and registration data for your Notified Body, Service Providers (e.g. Electrical Safety Certificate), Country Sponsors, Distributors, and more.
Maintain regulatory information
Medical device classifications and other regulatory information vary by country and product. If you can’t easily find this information in your own system, how efficient can you be getting products to market?
Eliminate the administrative functions of regulatory affairs by eliminating inefficient and manual processes.