Surprise Revelation In EU Guidance On Equivalence In Clinical Evaluations Will Save Time And Money

EU guidance explaining the permissible use of equivalence in clinical investigations is well worth a read. It could significantly speed up a manufacturer’s regulatory journey, saving time and money.

Manufacturers reading the latest guidance document from the European Commission’s Medical Device Coordination Group on clinical evaluations and investigations are in for a welcome surprise.

Contracts, it says, are never required when a company claims equivalence of its products with another firm’s device. This is...

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