Save money and time, get standardized analysis
Analyses from the same vendor for 19 different EU countries
We will help you navigate through the challenges of reimbursement and funding for medical devices and in-vitro diagnostics in Europe
MTRC is a unique provider of Pan-European reimbursement services and products for Med Tech and IVD industry
MTRC is a unique provider of Pan-European reimbursement services and products for Med Tech and IVD industry
Scope
Coding, payment mechanism, reimbursement tariffs, pathway to create or improve reimbursement situation
Project-based on-demand work or >95 off-the-shelf syndicated reports
Countries
19 EU
Availability
Mixed
Scope
Seminars on introduction into market access for medical devices and IVD tests, seminars on reimbursement systems in individual countries (>60 reports)
Syndicated analytical reports on the topics of HTA, innovation funding, reimbursement of health apps
Countries
19 EU
Availability
Off-the-shelf
Scope
Fact-based approach to determine evidence requirements, based on the prevision reimbursement decisions
Countries
Europe
Availability
On demand
Scope
Subscription service with email alerts about initiated or published health technology assessments of medical devices and in-vitro diagnostic tests from 47 HTA organizations globally
Countries
18 countries globally
Availability
On-demand
Why us?
Pharma approach is put aside
Work with a company truly specialized in medical devices and diagnostics
Getting results instantly (reports) or within 4-8 weeks (services)
Make business decisions quickly
13 out of top-30 companies choose MTRC for reimbursement support
Work with a provider who understands industry’s needs
More than 110 projects accomplished during the last year
Work with a provider who has experience in your field
Team of 15 specialists in 6 countries
Work with a provider with a Pan-European capacity
More than 200 internal instructions and protocols
Be sure about quality of the results
To stay up-to-date, we daily monitor developments of reimbursement systems in Europe
Subscribe to our newsletter to get updates every 2nd week
27 Jul 2020
For the last three years, MTRC maintained a be-weekly newsletter with information about reimbursement and market access changes in European countries. From July 2020, we are extending this activity with an introduction of the paid subscription service HTA Alerts. It will include bi-weekly reports about initiated or published HTAs from 47 HTA organizations worldwide. Reports will be customized so that the clients receive notification for only relevant technologies.
05
Aug 2020
In July 2020, two new apps entered the level 1 of the mHealthBelgium validation pyramid. Healthentia is an eClinical platform to record Real World Data, that can be used either in clinical trials or by healthy individuals. Sunrise (class IIa) sleep testing device allows rapid and at home diagnosing respiratory sleep disorders.
04
Aug 2020
The Clinical Coding and Schedule Development (CCSD) group develops and maintains procedural and diagnostics nomenclature for private payers in England. New procedure codes concern planning, insertion, and removal of high/low dose rate radioactive treatment (brachytherapy) into a prostate tumor, open/laparoscopic repair of Spigelian hernia, and others. The codes are introduced with a recommended adoption date being the 1st of August 2020. The document also contains a list of textual changes in codes and unacceptable combinations. There were no changes to the CCSD Schedule of Diagnostic Tests.
03
Aug 2020
In June 2020, santésuisse (the leading organization of Swiss health insurers) and the Swiss Society of Surgeons (FCMH) have submitted a proposal to the Federal Council for the acceptance of 67 lump-sum payment packages for out-patient services. In July 2020, eight more lump-sum payment packages were suggested to the Federal Council. More suggestions are expected in the near future.
31
Jul 2020
In June 2020, the Andalusian Health Technology Assessment Department (AETSA) published an update of the earlier report (2012) on assessment of effectiveness and safety of tumor treating fields (TTF) therapy in glioblastoma.
Our two core services are the provision of off-the-shelf and on-demand reimbursement analysis and the development of reimbursement strategy for medical devices in 19 European countries
| Analysis | |
Reimbursement
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National fundingWillingness to pay for technology, based on:
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| Strategy |
Reimbursement strategyPathway to get reimbursement:
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Check our specific propositions for: Med Tech industry, IVD industry, Investors
Our services cover 19 European countries, including Austria, Belgium, Czech Republic, Denmark, England, Finland, France, Germany, Hungary, Italy, the Netherlands, Norway, Poland, Romania, Russia, Spain, Sweden, Switzerland and Turkey
We provide services for major types of medical technologies
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Implantable devices |
Interventional procedures |
Non-interventional procedures |
In-vitro diagnostic tests |
Medical aids |
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Our analytical team has worked on hundreds of reimbursement projects within different clinical and technological areas, including heart valve replacement, minimally invasive and open heart surgery, coronary, cerebral and peripheral stenting, coronary diagnostic and imaging techniques (fractional flow reserve, intravascular ultrasound), coronary, cerebral and peripheral vascular thrombectomy, implantable and extracorporeal ventricular assist devices, clinic- and home-based dialysis, extracorporeal membrane oxygenation, apheresis, obesity surgery, hernia and reconstruction surgery, tissue products and skin reconstruction surgery, negative wound pressure therapy and medical bandages, neurostimulators for different indications, cell therapy, rehabilitation devices, devices for minimally invasive and open spine surgery, embolization procedures, glucose monitoring, use of fusidial markers, radiotherapy, endoscopy and more
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Confidence in results
We have established numerous procedures and services to ensure the high relevance and precision of our analysis in order to successfully guide your business decisions:
- Standard Operating Procedures and Work Instructions
- Access to official coding and DRG manuals, tariff lists and grouping software
- A team comprised of experienced Clinical Coders with a medical background
- Quick access to health authorities to address uncertainties
- Ongoing research program to get insights from payer and provider interviews
- All reports are reviewed by the CEO before release
Check out our database of the off-the-shelf reimbursement reports for medical technologies in 11 European countries
Released reports:
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Ongoing reports:
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