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Ophthalmological procedures

23
Oct 2019

Summary of the HTA, funding and innovation payment landscape for ophthalmology technologies in Europe

MTRC has developed three reports on the key market access topics, including innovation funding, health technology assessment and funding frameworks for medical devices. These reports help to understand the relevance of these frameworks to certain types of medical technologies, including ophthalmology technologies. This post provides some key facts about the HTA, funding and innovation payment landscape for ophthalmology devices in Europe.
29
Jan 2019

Five new procedure codes added to private reimbursement schedule in England in October/November 2018

The Clinical Coding and Schedule Development (CCSD) group develops and maintains procedural and diagnostics nomenclature for private payers in England. In October/November 2018, five new procedure codes for laser correction of refractive error following non-refractive ophthalmic surgery, insertion of urethral catheterization device, injection of botulinum toxin for hyperhidrosis, laparoscopic and robotic-assisted pancreatoduodenectomy have been added to the CCSD Schedule.
25
May 2018

The call for a tender to conduct a pilot study “Transcorneal Electrical Stimulation in Retinitis Pigmentosa” was announced by the Federal Joint Committee (G-BA) at the end of April of 2018

On the 26th of April of 2018, the Federal Joint Committee (G-BA) has announced the call for a tender for the pilot study “Transcorneal Electrical Stimulation in Retinitis Pigmentosa” in the Official Journal of the European Union. The deadline for the requests is the 22nd of June, 2018, 14:00
29
Sep 2017

The Federal Joint Committee (G-BA) has prepared the path for a trial of the transcorneal electrical stimulation for retinitis pigmentosa in Germany

After successful trial application by the manufacturer (Okuvision) of a stimulation technology (Okustim), the Federal Joint Committee (G-BA) decided on a trial guideline for a co-funded study defining the key points of the planned study, including type and time period of the study, target population and control intervention. Results from the trial will be evaluated and may lead to reimbursement of the method in both, the inpatient and outpatient sectors.