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Post-Market Clinical Follow-up Studies (PMCF)

Many manufacturers face the fact that they are lacking clinical evidence even for devices that have been on the market for many years, at the risk of losing the CE-mark.

Conducting PMCF studies may represent significant budgets for medical device manufacturers to the point that some are weighing the burden against withdrawing their devices from the market.

MD-CLINICALS specialises in setting up rationalistic plans for PMCF to optimize costs while still delivering the necessary clinical evidence through solid data and keep devices on the market in compliance.

Before you risk losing the EU market:

Contact us for a free one-hour consultation