We offer high quality regulatory and marketing authorisation services for your medicinal products.
How we can help you with Regulatory Affairs
We mainly evaluate, but also carry out translations of promotional materials into Norwegian, e.g. short product information texts, websites, meeting invitations, e-letters, presentations and folders/brochures on your human, veterinary and herbal medicinal products as well as for medical devices and cosmetics.
How we can help you with Marketing
Guidance according to Norwegian and European procedures and requirements.
How we can help you with Medical device
Pharmaceutical wholesale is an intermediary between the pharmaceutical industry and their customers by purchasing and distributing medicines to their customers.
How we can help you with Pharmaceutical wholesale
The most recent EU legislation on pharmacovigilance was implemented into Norwegian law in November 2013.
How we can help you with Pharmacovigilance
Good Manufacturing Practice (GMP) describes the standards that a pharmaceutical Marketing Authorisation Holder/Manufacturer must meet to ensure that the quality and integrity of the medicinal products is maintained at the release of the products, to the supply chain and through the product’s lifetime. According to EU law, the Marketing Authorisation Holder must permanently and continuously have at his disposal the services of at least one qualified person.
How we can help you with QP-services
Mericon do also offer other services related to non-pharmaceutical product areas.
How we can help you with Other services