Solutions

We have a solution for everything – and the corresponding experience. In our current seven areas of expertise, we are at your disposal with our comprehensive know-how.

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Software

Software

With our PAS-X Manufacturing Execution System (MES) and software solutions for Analysis, Track & Trace, Networked Factories, and Intelligent Packaging, we are the world's leading supplier and partner to the pharmaceutical and biotech industries.

Overview Software

Handling

Handling

We are specialists for complete handling systems for pharmaceutical and medical products. Our solutions are decisive in the field of contactless and safe transport of e.g. glass syringes.

Overview Handling

Inspection

Inspection

As the world's leading inspection expert, we develop solutions for the pharmaceutical and biotech industries. Our range of products extends from high-performance machines and semi-automatic machines to laboratory units and inspection applications for in-process control.

Overview Inspection

Packaging materials

Packaging materials

As long-standing specialists, we develop packaging solutions for innovative and high-quality secondary pharmaceutical packaging made of cardboard. We offer you solutions for counterfeit protection, standard folding boxes and much more.

Overview Packaging materials

Services

You need help with a specific product or have questions about one of our areas of expertise? Take advantage of our extensive range of services, we will support you quickly and easily.

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Packaging materials

Packaging materials

The demands on pharmaceutical packaging are high: it should be forgery-proof and childproof, but also compact and sustainable. Find out here how we make packaging future-proof.

Overview Packaging materials Services

About us

We at Körber in the Pharmaceuticals business area are the people to contact when it comes to pharmaceutical products. As a leading system provider, we advise our customers from the development and production to the inspection and packaging of their products.

All about us

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Track & Trace

Updated: Delegated Regulation (EU) 2016/161 – Questions and Answers Version 10

For this reason, the European Commission, as executive organ of the EU, published the 9th version of the FAQ document "Safety Features for Medicinal Products for Human Use". We are pleased to keep you up-to-date on this topic. The current version is available here.

Background:

The European Commission released the "COMMISSION DELEGATED REGULATION (EU) 2016/161 of 2 October 2015". The regulation describes a system, which allows for an "end-to-end" verification of medical products bearing the safety features. "In practice, the authenticity and integrity of the safety features placed on the packaging of a medicinal product at the beginning of the supply chain should be verified at the time the medicinal product is supplied to the public, […]."

The transition period started now, for most of the European countries (almost all) prescription drugs must bear the features from 9th of February 2019 onwards. Talk to us on this topic, raise your questions on this regulation, and discuss your business needs with us.

Link to English regulation: eur-lex.europa.eu/legal-content/EN/TXT/PDF/

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