News - Marketing authorisation medicines for human use
23 news items Marketing authorisation medicines for human use
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Revised notification form for medicine shortages and defects
The notification form of the Medicine Shortages and Defects Notification Centre has been made more user-friendly. The marketing ...
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Planning tool for requesting timeslots expanded to more procedures
The planning tool firms can use to reserve a timeslot for requesting assessment procedures is being expanded. From now on, the ...
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MEB fee rate change as of January 2024
The Medicines Evaluation Board (MEB) increases the fee rates for authorisation applications, authorisation changes and the annual ...
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Changes to fees for human medicinal products and devices as of 1 January 2023
With effect from 1 January 2023, the Medicines Evaluation Board (MEB) will be increasing the fees for authorisation applications, ...
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All MEB correspondence on human medicines will in future be sent by email
From 1 July 2022, all correspondence from the Medicines Evaluation Board on human medicines will be sent by email. Correspondence ...
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Amended policy on national implementation of additional risk minimisation measures
The Medicines Evaluation Board (MEB) has amended its policy for the national implementation of additional risk minimisation ...
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Medicines available faster due to simultaneous assessment
The National Health Care Institute joined forces with the Medicines Evaluation Board to develop a method that would give patients ...
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Improvements to the notification process and form now available
In December 2021 the Medicines Evaluation Board and the Health and Youth Care Inspectorate announced the introduction of changes ...
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MEB fee rate change as of January 2022
The Medicines Evaluation Board (MEB) increases the fee rates for authorisation applications, authorisation changes and the annual ...
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Changes to policy on product information
The Medicines Evaluation Board (MEB) has recently revised two policy documents for pharmaceutical companies in respect of the ...