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Packaging technology in the pharmaceutical industry
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Packaging technology in the pharmaceutical industry

General Information

Lecturer: Prof. Klaus Dilger, Dipl.-Chem. Elisabeth Stammen
Start: see StudIP
Degree: Master
Credit points: 5Module number: MB-IPAT-43 
Rotation: summer semester

To the exam dates

Support

Elisabeth Stammen
+49 241 - 963 2706
e.stammen(at)tu-braunschweig.de

Qualification goals

Verpackungstechnik

The lecture "Packaging technology in the pharmaceutical industry" is part of the module: "Quality control, hygienic design and packaging technology".

The primary (e.g. tubes, blisters, ampoules) and secondary packaging (e.g. cardboard boxes) of pharmaceutical products are closely related to their production and are an integrated part of the value-added process.
Packaging processes are associated with a high risk due to the large number of quality and safety-critical influences. These include the complex mechanics of the systems, the variety of products and packaging variants, as well as the correct attachment of variable data and the necessary measures to prevent counterfeiting.

Containment includes both product and personal protection. Highly active and sensitive products are increasingly being used in the pharmaceutical sector. On the one hand, this requires new, more complex packaging materials and their processing on suitably designed equipment, but on the other hand, personal and product protection during packaging must also be taken into account.convenience means user-friendliness. The competition is particularly fierce in the area of over-the-counter products; a user-friendly form (also with regard to child safety, seniors' friendliness or dosage form for chronically ill patients) can be decisive for the market.counterfeit protection is particularly important for special preparations (cancer drugs etc.). The originality of the drug must be protected in order to guarantee effective action; counterfeiters and fraudsters are stopped by track and trace, RFID identification, design solutions, etc.

After completing this module, students will have mastered the most important basics about the different types of primary and secondary packaging in the pharmaceutical industry. They learn the legal principles and requirements for pharmaceutical packaging with regard to quality assurance. By looking at clear examples, the students are able to understand the complex process chain, taking into account the implementation of the above requirements, and have mastered the essential knowledge to implement them.

Content

Mediation of the basics and consolidation

  • Introduction, basic terms, definitions and market overview
  • Primary packaging I & II
  • Automation in the pharmaceutical industry
  • Packaging for non-tablet products
  • Packaging machines for tablets
  • Secondary packaging I & II
  • Summary, repetition and exam preparation

Lecture notes & Downloads

Lecture notes are available to participants via  StudIP.

 

 

Literature

The following textbooks offer a deeper insight into the contents of this lecture.

  • Günter Bleisch, Jens-Peter Mayschak, Uta Weiß: Verpackungstechnische Prozesse; ISBN 978-3-89947-281-3
  • Michael ten Hompel, Thorsten Schmidt, Lars Nagel: Materialflusssysteme; ISBN 978-3-540-73235-8
  • Lothar Gail, Udo Gommel, Hans-Peter Horting (Hrsg.): Reinraumtechnik; ISBN 978-3-642-19434-4

Module Manual

Only the information in the module manual applies. In addition, only the information in the examination regulations of the respective course of study is legally binding.

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