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Compliance In Packaging

– Ensuring Quality and Control Throughout the Supply Chain

QUALITY MANAGEMENT AND TRACEABILITY

At ApodanNordic PharmaPackaging, quality assurance and process control are integrated throughout the entire supply chain. Our quality management procedures are based on GMP principle (Good Manufacturing Practice) to support the requirements of the pharmaceutical industry and diagnostic packaging applications.

A large share of our glass and plastic pharmaceutical containers is produced in controlled cleanroom environments and supplied in hygienic packaging conditions to support product integrity and handling safety.
Our rubber stoppers can be delivered with rinse and sterilization using WFI (Water For Injection) and packed in sterilized bags for autoclaving or direct integration into production processes.

Standards and Documentation

ApodanNordic PharmaPackaging supplies pharmaceutical packaging components manufactured according to applicable ISO and DIN standards. Production and material specifications are aligned with current European Pharmacopoeia (Ph. Eur.) monographs to support consistent product quality and regulatory documentation requirements. Documentation is provided through relevant test certificates and supporting quality documentation.

Our quality procedures include:

  • Batch registration for traceability
  • Defined packaging specifications
  • Documented control and quarantine procedures

We call this Compliance in Packaging. Compliance in Packaging reflects our approach to quality control, documentation, and supply reliability within pharmaceutical packaging.

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PART OF AN INTERNATIONAL NETWORK

ApodanNordic PharmaPackaging is a part of an international network, enabling us to offer even more than what you will find on this website. 

ApodanNordic PharmaPackaging is a subsidiary company to Fagron, which is represented in large parts of the world, enabling us to deliver almost everything our customers may demand – in a timely manner! 

Read more about Fagron here.

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