TRAINING
Clinical Evaluations
Manufacturers struggle to address requirements for clinical evaluation for all classes of devices, with many erroneously assuming class I devices will not need clinical data. Clinical evaluation is required for all medical devices regardless of risk classification or clinical data requirements.
TRAINING
Why choose Qserve as your trainer?
We offer a comprehensive program of training courses on a wide range of regulatory, clinical, Our courses are delivered by our experts and are suitable for professionals at all stages of their career.
As a leading medical device consultancy with offices in Europe, the United States, and China. Qserve's staff offers years of international experience with both broad and specific expertise for a wide range of medical devices and IVDs.
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