3.1
Clinicians must report any instances of intraocular lens removal because of adverse events to the Medicines and Healthcare products Regulatory Agency (MHRA).
Guidance
3 Further information
3.2
NICE has published interventional procedures guidance on several procedures relating to refractive error and IOL insertion. For more information, see our webpage on NICE interventional procedures guidance.
Sources of evidence
The evidence considered by the Interventional Procedures Advisory Committee is described in the overview.
Information for patients
NICE has produced information for the public on this procedure. It explains the nature of the procedure and the guidance issued by NICE, and has been written with patient consent in mind.
ISBN: 978-1-4731-6298-3