News
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Time to Update Your Veterinary Product Information
In the veterinary pharmaceutical industry, staying up to date with current regulations is essential for ensuring your medicinal products remain compliant. With regulations continuously evolving, it's important to ensure your product information aligns with the latest requirements. Since the Veterinary Medicinal Products Regulation (EU 2019/6) came into force in January 2022, it has been mandatory to use QRD template version 9 for all new marketing authorisation applications. This brings new obligations for both new and existing marketing authorisations.
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Farmasidagene 2024 – Meet Us at Our Stand
Mericon will be attending Farmasidagene 2024, and we are excited to meet both new and familiar faces. At our stand, you will also meet Janne Høiset, head of the Marketing Compliance team, who will be available to answer your questions.
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Regulatory Changes for Medical Devices Adopted by the EU Commission
The EU Commission has introduced regulatory changes to in vitro diagnostic medical devices (IVDR), including extended transitional periods to ensure a steady supply in the European market.
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Thank you for your dedication
We would like to extend our heartfelt thanks to Már Steinsen, who retired this summer after a long and impressive career within the Pharmaceutical industry, and the last years as a member of our staff.
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Are you looking for reliable and professional scientific and medical writing services?
At Mericon, we offer tailored services for researchers, healthcare professionals, and organizations that need accurate and compelling content. Our team of experienced writers and researchers ensures that your work is presented in the best possible way, whether through research articles, medical reports, or other scientific communications. Learn more about our scientific and medical writing services […]
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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.