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Evaluations completed: April 2018 to March 2019.
How to conform with the legal requirements for placing medical devices on the market.
This document sets out the standards, reporting guidelines and evaluation criteria for cytopathology in cervical screening.
The MHRA has conducted an assessment following reports of osteolysis and early device failure in the literature and is issuing new monitoring requirements for patients implanted with the M6-C artificial cervical disc.
External quality assessment scheme for the preparation and staining of cervical liquid based cytology samples.
How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
The VDEC clinical evaluation team works to support vaccine and therapeutic development by providing expertise in immunological and functional assays used to support clinical trials (Phase I to IV)
An MHRA investigation has found increased risks of wear and corrosion, including an increased occurrence of device fracture and revision surgery associated with cobalt chrome-containing Profemur modular neck hip stem components.
Helping public health practitioners conducting evaluations – identifying when it is possible and appropriate to evaluate.
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