FDA approves Artivion’s AMDS device PMA
The approval was based on data from the PERSEVERE US IDE trial, which included 93 participants.
Educating the medical device manufacturing industry since 2002.
The approval was based on data from the PERSEVERE US IDE trial, which included 93 participants.
To track and verify embodied emissions through every stage of the supply chain, leading OEMs are piloting blockchain-anchored digital product passports (DPPs). Ellie Philpotts talks to Chris Taylor, sustainability lead...
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