U.K. seeks advice from device firms over neurostimulator guidance

08/7/2009 | Clinica (subscription required)

The U.K.'s Medicines and Healthcare products Regulatory Agency is seeking consultation with medical-device companies in regard to a draft guidance on reporting adverse events related to neurostimulators. The consultation on the guidance, which intends to streamline the application and enforcement of the medical devices directive 93/42/EEC, is set to close at the end of September.

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