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Articles tagged with: Ministry of Health
Action Required in the Database for Legacy Devices
The Ministry of Health has defined mandatory actions for updating legacy device registrations in the database.
29/02/2024
Matteo Valtorta
Deadlines and exemptions
Ministry of Health
5.5% Contribution for Promotional Expenses, the Guide
By April 30th of each year, it is mandatory to declare promotional activity expenses and pay the 5.5% contribution to the Ministry.
20/07/2022
Matteo Valtorta
Advertising
Deadlines and exemptions
Manufacturers' duties
Medical Device Vigilance: Ministry Guidelines
A new circular from the Ministry defines the methods for medical device vigilance while waiting for Eudamed to become operational.
04/05/2022
Matteo Valtorta
Ministry of Health
Surveillance and vigilance
Action Required in the Ministry’s Database
After the latest modification to the medical devices database, action is required to update existing registrations. The details.
13/01/2022
Matteo Valtorta
Deadlines and exemptions
Ministry of Health
Registering Medical Devices in the Ministry’s Database
While waiting for Eudamed, registration in the Ministry's database remains mandatory. This includes devices under MDR.
29/09/2021
Matteo Valtorta
Deadlines and exemptions
Ministry of Health
The CND, when Italy is Top of the Class in Europe
The European Commission has decided to adopt the Italian National Classification of Devices as the official nomenclature in Eudamed.
22/04/2021
Matteo Valtorta
Eudamed
Ministry of Health
Servizi
European Medical Device Regulation Consulting
CE Marking for Medical Devices
ISO 13485 and MDSAP Quality System
Technical Documentation
UDI and Eudamed Registration
Training Courses
European Medical Device Regulation Consulting
CE Marking for Medical Devices
ISO 13485 and MDSAP Quality System
Technical Documentation
UDI and Eudamed Registration
Training Courses
Home
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Home
Company
Work Method
Blog
Contact
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Services
European Medical Device Regulation Consulting
CE Marking for Medical Devices
ISO 13485 and MDSAP Quality System
Technical Documentation
UDI and Eudamed Registration
Training Courses
European Medical Device Regulation Consulting
CE Marking for Medical Devices
ISO 13485 and MDSAP Quality System
Technical Documentation
UDI and Eudamed Registration
Training Courses
Home
Company
Work Method
Blog
Contact
Home
Company
Work Method
Blog
Contact
English
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