QMS (Distributors) Returned Equipment Requirements Package
The Returned Equipment package, as a part of the Quality Management System (QMS), has been developed for distributors of Medical or In Vitro Diagnostic (IVD) devices. The Returned Equipment package contains the Returned Demonstration Equipment Procedure. The package is compliant with ISO 13485:2016, EU MDR 2017/745, and EU IVDR 2017/46. (number of documents – 1)
- SOP 5.1 Returned Demonstration Equipment Procedure
Please note that once purchased, the product cannot be returned or refunded.
Big Bundle Packages as well available: