Support in the preparation of the Medical Device Technical Dossier and its respective regulatory submission.
Descrição
This consulting service provides guidance in preparing the Technical Dossier for Medical Devices, including usability tests, clinical trials, risk analysis, instruction manual, data flow and processes, as well as support the submission to the regulatory agency.
Key-words
Regulatory consulting
Medical devices
Technical dossier
Service Information
outros
Segment
on demand (incubation - physical space)
Delivery Format
2ca@ccabraga.org
Contact