[E14-11] Transcorneal electrical stimulation for retinitis pigmentosa (Addendum to commission E14-07)

Within the framework of the testing regulation the Federal Joint Committee (G-BA) can commission IQWiG to assess the potential of a new examination or treatment method (i.e. of a medical device). As part of an administrative procedure conducted by the G-BA, the topics and content of the assessments of the potential of medical devices are confidential until the testing directive is passed.