3.1 Clinicians must report any instances of intraocular lens removal because of adverse events to the Medicines and Healthcare products Regulatory Agency (MHRA).
3.2 NICE has published interventional procedures guidance on several procedures relating to refractive error and IOL insertion. For more information see our website.
NICE has produced information on this procedure for patients and carers ('Understanding NICE guidance'). It explains the nature of the procedure and the guidance issued by NICE, and has been written with patient consent in mind.