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Radiopharmaceutical Adverse Events and Product Defects reporting

All serious adverse events should always be reported via the MHRA and CHM (Commission on Human Medicines) portals:
 
YELLOW CARDS:  for serious pharmaceutical adverse events; see
 
BLUE CARDS: for medical devices adverse incidents; see
 
BNMS professional-led database for non-critical adverse events and product defects,  can be found here: