ISO 11607 and MDR | Medical packaging development

Demonstration of fitness for purpose is a vital element of any new product or pack development program. For medical packaging however, this is a mandatory regulatory requirement before a product can be placed on the market. From the Medical Device Regulation (MDR) and ISO 11607, to assurances of transit performance, see how careful consideration needs to be taken when developing medical packaging. Find out more in the article below.

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