Organisations who needs to onboard the Swedish system (SMVS) fills in the request (only available in Swedish).
Concerns end users such as Pharmacies, Wholesalers etc.
Do you need to onboard? See information
The form consists of three parts and all fields need to be filled in for the request to be submitted.
Requests will be handled within a few working days.
Each Marketing Authorisation Holder (MAH) which markets at least one product covered by the Falsified Medicines Directiv (FMD) within a national territory must have a contract with the National Medicines Verification Organisation (NMV) in Sweden e-VIS.
For questions regarding MAH contracts please contact firstname.lastname@example.org
When you fill in this form, all details, including your personal details, will be saved and handled by e-VIS. This is necessary for e-VIS in order to onboard you to the system.
All personal details are treated confidentially and according to the Data Protection Regulation (EU) 2016/679. You are entitled to access the information collected by e-VIS. If you wish to be informed about the information, or if you want to request correction for incorrect information, you shall in writing send this request to e-VIS, c/o LIF Service AB, P.O. Box 17608, SE-118 92 Stockholm or info@e-VIS.se