QMS (Distributors) Visitors Requirements Package
The Visitors package, as a part of the Quality Management System (QMS), has been developed for distributors of Medical or In Vitro Diagnostic (IVD) devices. The Visitors package contains the Record of visitors and requirement Procedure. The package is compliant with ISO 13485:2016, EU MDR 2017/745, and EU IVDR 2017/46. (number of documents – 1):
- SOP 4.8 Record of Visitors and Requirement Procedure
Please note that once purchased, the product cannot be returned or refunded.
Big Bundle Packages as well available: