Safety and quality
As a pharmaceutical business in the Nordics, we have a responsibility towards patients, pharmacies and hospitals and we, therefore, strive to do our best to avoid mistakes. We never compromise on quality. Being in the top 3 in Denmark, Sweden and Finland and handling well over 800 different products in several international locations, means a need for strict quality procedures and documentation on every action taken.
Our team secures quality in every step
Our local regulatory team has more than 20 experts, all with a medical background who ensure that all the right procedures are followed in every step from notifying the original manufacturer, through licensing, repackaging, patient information leaflet, controls and production to the release on the national market. During the production, we perform a quality control of each batch, and furthermore, we make audits on suppliers, repackaging, storage, and transport contractors.
Apply to all EU regulations
All Paranova products correspond to those that are distributed by multinational pharmaceutical companies in Denmark, Finland, Norway and Sweden and are under constant scrutiny by the responsible national Federal Institute for Drugs and Medical Devices. To guarantee the safety and quality of the medicinal products, for years Paranova Group A/S and MPA Pharma group have worked closely with trusted suppliers in EU countries and have performed qualification of suppliers before the products are delivered. Furthermore, Paranova Group A/S and it affiliates are audited every second year by the national authorities.
Big network means big advantages in safety
The collaboration in the MPA Pharma group streamlines procedures, and we benefit from their investment in a modern refrigerated warehouse of 1,000 square meters. Here, large quantities of reimported and parallel imported medicinal products are repackaged, a process during which the cold chain may not be interrupted. The European Commission is currently preparing to introduce even stricter transportation regulations for medicinal products. We are ready to meet the new requirements thanks to our logistic partners who provide us with temperature-controlled transportation services.
Questions about safety features on packaging
(2D code, human-readable format, anti-tampering device)
Pakkausten turvaominaisuuksiin liittyvät kysymykset (FI)
(2D-koodi, silmin luettava muoto, peukaloinnin paljastava mekanismi)
puh. +358 9 4391 850
ma-pe klo 9-16
Spørsmål som vedrører sikkerhetsanordninger på legemiddelets forpakning (NO)
(2D-kode, lesbar informasjon, sikkerhetsforsegling)
Tel.: +45 44 74 61 62
Man-Fre kl.: 8-16
Spørgsmål som vedrører sikkerhedsanordninger på lægemiddelpakninger (DK)
(2D-kode, læsbar information, sikkerhedsforsegling)
Tlf.: +45 44 74 61 62
Man-Fre kl.: 8-16
Frågor gällande säkerhetsdetaljer på läkemedelsförpackningar (SE)
(2D-kod, läsbara information, säkerhetsförsegling)
tel. +46 8 446 30 30
må-fre kl 9-16