QMS (Distributors) Feedback Requirements Package
The Feedback package, as a part of the Quality Management System (QMS), has been developed for distributors of Medical or In Vitro Diagnostic (IVD) devices. The Feedback package contains the Feedback Procedure, and 1 related Template. The package is compliant with ISO 13485:2016, EU MDR 2017/745, and EU IVDR 2017/46. (number of documents – 2)
- SOP 5.6 Feedback Procedure
- T 5.6-1 Customer Satisfaction Questionnaire
Please note that once purchased, the product cannot be returned or refunded.
Big Bundle Packages as well available: