compliance
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Updated Guidelines on Pharmaceutical Marketing – What Does It Mean for You?
On December 19, 2024, the Norwegian Medical Products Agency (NOMA) published updated guidelines on pharmaceutical marketing regulations. These updates are intended for the pharmaceutical industry, pharmacies, clinics, and other entities involved in marketing medicinal products for humans and animals. The revised guidelines introduce important changes, both linguistic and structural. Why Is This Important? Pharmaceutical marketing […]
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Keep Your Product Information Updated – Avoid Outdated Package Leaflets!
The pharmaceutical industry faces constantly evolving regulatory requirements, making it crucial to ensure that product information aligns with the latest standards. This includes updating according to QRD and removing outdated "blue box" statements from the package leaflets.
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Effective and compliant marketing of pharmaceutical products
Are you looking to market your pharmaceuticals in the most effective way possible while complying fully with the regulatory framework? Marketing authorisation holders must set up a scientific service staffed by employees with the requisite training and expertise to provide information about the company’s pharmaceutical products. So you may wish to consider outsourcing the quality assurance of your pharmaceutical communications.
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Contract Responsible Person (RP/FFA)
Mericon AS can offer support to every aspect of your distribution and supply chain, including Contract Responsible Person (RP/FFA).
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How to label food supplements?
Are you launching a food supplement on the Norwegian market? Do you need help labeling your product correctly ?