In February this year, the European Parliament approved the EU Directive on Cross-Border Healthcare, establishing a framework for patients to exploit their rights to healthcare in other European countries.
When the European Parliament voted in favour of the EU Directive on Patients’ Rights in Cross-border Healthcare, Health Commissioner John Dalli, explained that this is an important step forward for all EU patients – i.e. by gaining easier access to good quality and reimbursed treatment across EU borders. Meanwhile, Europe’s healthcare systems will need to deliver ‘more for less’.
Two serious new laws were passed at the end of 2010, one regarding obligatory medical insurance the other the ‘83 Federal Law’, which changes the rules of State regulation of the social sector. Some experts believe that the 83 FL will be the death warrant for accessible education and healthcare in Russia.
Whether it’s functional imaging via MRI or CT, dynamic angiography examinations or volume tomography -- new examination procedures deliver more, but also require more. The annual data increase in hospitals is 20-30% and the resulting requirements for the necessary storage capacity, or for digital data transfer, present a serious challenge. Accordingly, there is considerable interest in…
Yes, cancer research is making rapid progress, but -- how can the transfer of cancer research into successful treatments be accelerated? In Berlin this October, that vexing question was up for discussion during the European Forum on Oncology. Also on the agenda: How best practice approaches to cancer therapy can be adopted throughout the European Union.
For some time, German pathology has only been in the background of the medical disciplines. However, during the last ten years the profession stepped up to the fore. In the face of molecular medicine developments, the German Association of Pathologists redefined its members position with revived self-confidence.
Different tests bring different results, and results of the same types of test vary from laboratory to laboratory. "In the case of test procedures for autoimmune diseases there are incredible discrepancies," confirmed Professor Manfred Herold, head of the Laboratory for Rheumatism at the University Clinic for Internal Medicine One, Innsbruck. The reason: "There are no standards for…
Changing for the better does not depend on the number of hospitals, physicians or beds you have; it’s about eliminating inefficiencies in the pathways of patient care. The organising principle for healthcare needs to be quality. ‘It is the one industry where quality is cheaper,’ emphasises Ari Darzi, renowned pioneer in minimally invasive and robotic surgery, holder of the Hamlyn Chair of…
250 delegates from some 30 countries arrived in Hamburg this November to discuss e-health and share knowledge from their own countries at the first Global E-Health Forum and discuss.
"Some progress, but the big challenges remain". This was the verdict after the European Society of Cardiology (ESC) hosted the 2010 European Summit on CVD Prevention on 30 November. The summit was attended by a broad cross-section of medical experts, healthcare organisations, national societies, regulators and representatives from the European Union (EU). The aim of this bi-annual event is to…
COCIR* issued an easy-to-use tool to help determine whether software is a medical device or not. Since the revision of the European Medical Device Directive, in force as of 21 March 2010, the definition for medical devices also includes software used for diagnostic and therapeutic purposes. In December 2009, the European Commission decided to develop a European guidance document to clarify which…
Held every three years, a very important healthcare IT event is to be held in Europe after a gap of 14 years. From November 15-19, healthcare managers and suppliers from 37 countries will arrive in Milan to discuss the future of world’s electronic health services at the 16th Congress of IFHRO (International Federation of Health Records Organisations), held in collaboration with the WHO.
During the 2010 ESC meeting, held in Stockholm, new guidelines for myocardial revascularisation were handed down by a prestigious Task Force made up of representatives of both the ESC and the European Association of Cardio-Thoracic Surgeons (EACTS).
One year after boldly launching a far-reaching programme for reforming France’s troubled hospitals a newly created French agency has surprised its detractors and created a way forward.
Today, healthcare professions make up ten percent Europe’s workforce. The EU Commission calculates dramatic shortages in healthcare provision in the next decade unless countermeasures are taken now. Thus, at this year’s European Health Forum Gastein (EHFG), held in October in Bad Hofgastein, Austria, international experts discussed ways to make health employment more attractive.
Given that European countries have very diverse healthcare systems with special types of hospitals and even special information systems, comparison of healthcare systems and hospital performances is difficult. Thus, the first HIMSS Europe Leadership IT Summit, which took place in Rome, has provided a platform from which to discuss quality patient care based on IT and particularly the…
Facing the risk of an invasion by big international operations, French medical laboratories drew inspiration for their defence from a national hero - Asterix. While the newly launched reform of the French laboratory system will bring the traditionally independent medical labs into conformance with international quality standards, the law builds an elaborate defence against foreign operators to…
How to finance the healthcare system? It’s an ongoing dilemma, particularly for in-patient care. According to a German Hospital Federation (DKG) estimate, the country’s hospitals currently suffer an investment backlog of €30-50 billion.
EU Commissioner for Health and Consumer Policy, John Dalli, presented some of his key health priorities today at the 13th European Health Forum Gastein (EHFG). Among the important topics on his agenda: prevention, in particular in the field of tobacco control; an appropriate framework for cross-border healthcare; and innovation in the field of active and healthy ageing.
The reprocessing of single use medical devices is well-established in Europe. However, questions about the risk for patients and users arise constantly. The European Commission presented recently a kind of risk survey. The report strikes German experts as basically accurate but unbalanced.
The accuracy and reliability of medical laboratory examination results are vital part in healthcare delivery, and these plus the effective operation of laboratories are the main goals of laboratory managers. To ensure a high quality operation, medical laboratories have quality management systems and, through laboratory accreditation, show their competence.
A Government White Paper on healthcare reform has caused Unison, Britain’s biggest public sector trade union (over 1.3 million members), to launch legal action against the Government ‘as a matter of urgency’. The day after the paper was presented in July, NHS CEOs were instructed by NHS CEO Sir David Nicholson to implement the proposals ‘immediately’ - without being given time to…
More than 600 distinguished guests from 40 countries are expected at this year’s European Health Forum Gastein (EHFG). ‘Since its foundation in 1998, the EHFG has developed into an international meeting point for the highest-ranking healthcare politicians, managers and scientists from all over the world,’ said EHFG President Professor Günther Leiner.
When Swiss orthopaedic surgeon Dr Marino Delmi, Past-President of the Swiss Foot & Ankle Society, Member of the Council of the European Foot & Ankle Society, and of the Scientific Foot & Ankle Council of the European Federation of National Associations of Orthopaedics and Traumatology (EFORT), met with other experts in the field, three critical diabetes topics were explored.
Eucomed, the European Medical Technology Industry association, welcomes the European Commission's (EC) report on the reprocessing of medical devices. While remaining typically neutral in terms of action at this stage of the debate, the EC report confirmed that even with all the evidence and scientific opinion available "...it is not possible to quantify the risk associated with the use of…
