At Herlev Pharma Service, we offer a comprehensive solution for the storage, repackaging, and handling of pharmaceutical products. Our facilities operate in compliance with EU-GMP, investigational medicinal Product (IMP) regulations, as well as rules for medical cannabis, ensuring high quality and compliance in all processes.
Repackaging may be required for various reasons, such as label changes, adjustments to packaging text, language adaptations, or other regulatory requirements. We offer a flexible and tailored repackaging service that ensures your products reach customers and partners quickly and accurately. Our Qualified Person (QP) can release products to the market in Denmark, the EU, and globally, always in full compliance with applicable regulatory requirements. We handle the entire documentation process, develop necessary SOPs, and establish a comprehensive quality agreement between Herlev Pharma Service and your company.
Our approved production facilities can handle secondary packaging, labeling, and the necessary documentation related to daily operations, ensuring you always have a reliable partner in your supply chain.
Our services include:
IMPORT From the manufacturing site (globally), including application for import licenses and related processes.
TRANSPORT We manage transportation to Denmark, including import and export licenses on your behalf.
RECEIPT INSPECTION We inspect products upon receipt to ensure that quality meets the required specifications. We can manage all types of analyses and related tasks through partnerships with analytical laboratories.
QUARANTINE Before release, products are stored in our approved quarantine warehouse.
HANDLING We carry out the agreed handling, which may include repackaging, clinical packaging, labeling, and more.
RELEASE We review all relevant documentation, batch records, etc., and carry out the product release. This may include standard release, EU release from a third country, medical cannabis, and more.
STORAGE We can store the products until they are ready for further distribution. Products can be stored at 15–25°C in our approved facility.
DISTRIBUTION We can handle the further distribution to recipient companies, clinical departments, wholesalers, as well as export to companies abroad.
In addition, we can undertake:
Destruction
Through our network of partners, we can find solutions for you if there is a need for repackaging in primary packaging or other tasks that require approval for handling open packaging.
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