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Injection Moulding

White Paper

Getting drug-device combinations to market

The key to getting drug-device combinations to market compliantly is in the classification of the product. But what other considerations are applicable?

White Paper

The must-know clinical evaluation requirements

With the new European Union Medical Device Regulation (MDR 2017/745) replacing the Medical Device Directive (MDD 93/42/EEC) in May 2021, the requirements for clinical evaluation have changed. Read our whitepaper to understand how you’re affected.