Article 16 of the European Union’s Medical Device Regulation and In Vitro Diagnostic Regulation specifically address the ...
In the medical device industry, FDA inspections are not a regulatory hurdle — they are a powerful tool for improving product quality, operational efficiency, and patient safety. Shift from a reactive ...
Experience the next generation of biopharma innovation with PharmaLok™ ZerO sanitary clamps. Designed to simplify and streamline biopharma processes, these advanced clamps feature a universal fit and ...
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