QMS (Distributors) Service Requirements Package
The Service package, as part of the Quality Management System (QMS), has been developed for distributors of Medical or In Vitro Diagnostic (IVD) devices. The Service package contains the Control of Service Procedure. The package is complied with ISO 13485:2016, EU MDR 2017/745, and EU IVDR 2017/46. (number of documents – 1)
- SOP 4.6 Control of Service Procedure
Please note that once purchased, the product cannot be returned or refunded.
Big Bundle Packages as well available: