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I am new to medical device packaging. Why do so many products have porous windows in their packaging even though they are not gas-sterilised?

There are legacy PVC medical device products on the EU market that have been used in large volume over at least the past three decades with, presumably, no deleterious effects. They would be expected to fail the current 10993 testing (as PVC is used as a

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What is your foremost professional concern in 2012

Eurozone economic issues

50%

Recast of MDD

Stricter regulatory requirements

50%

Unfair competition from low-wage countries

Changing business model

Total votes: 4

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Archived Webcast

Watch the archived free webcast "How to Achieve Compliance with IEC 62304 for Medical Device Software Development." Complying with the IEC 62304 standard for medical device software requires an established software lifecycle process that includes strong support for risk management and safety assessment. However, IEC 62304 compliance does not need to slow down your medical device software development.

MEDTEC Magazin

Volume 2

Februar 2011, Volume 2, No. 1

German-language MEDTEC Europe preview

Volume 1

Februar 2010, Volume 1, No. 1

MEDTEC Magazin is a German-language supplement dedicated to the MEDTEC Europe trade show held 23-25 March in Stuttgart. The publication also includes articles on the German economy, micro-technology and outsourcing.

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- Qmed - Qualified Medical Suppliers - Medical Device + Diagnostic Industry - IVD Technology - Medical Product Manufacturing News	- Medical Electronics Design - OrthoTec - China Medical Device Manufacturer - medtechinsider	- medtechinsider auf Deutsch - Pharmaceutical & Medical Packaging News - Pharmalive

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