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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, ISO 13485, IMP regulations, as well as rules for controlled substances (§39) and 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.
