Legemiddelverket
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About Legemiddelverket
The Norwegian Medicines Agency (DMP) ensures equitable access to effective medicines and medical devices. It oversees safety, promotes proper usage, and supports research and innovation in the field of medical products.
Access information about the approval and regulation of medicines and medical devices.
What You Can Do
- Learn about drug approval processes
- Explore guidelines for clinical trials
- Understand the status of various medicines
- Find information on generic and parallel-imported drugs
Frequently Asked Questions
What is the role of the Norwegian Medicines Agency?
The agency is responsible for ensuring access to safe and effective medicines and medical devices in Norway.
How are medicines approved in Norway?
Medicines are approved based on rigorous evaluation of their safety, efficacy, and quality.
What information can I find about clinical trials?
You can find guidelines and information regarding the conduct of clinical trials for medicines.
What is a generic medicine?
A generic medicine is a medication that is equivalent to a brand-name product in dosage, strength, and administration but is marketed under its chemical name.
How does the agency contribute to medical research?
The agency supports research and innovation to enhance the development of new medical products.