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The intention of the bill is to make it possible for providers of medical specialist care to distribute profits, under circumstances.

The Covid-19 pandemic has brought many changes to how we live our lives with altered daily routines, new ways of working and uncertainly as to how long it will last and what the future will look like.

On 23 September 2011 the draft of the e-labelling regulation that I wrote about earlier was discussed in the comitiology committee for the Medical Devices Directive.

Today I attended the COCIR workshop Regulating Medical Software in Brussels, a very interesting event that brought a lot of new information to my attention and I had the opportunity to speak to many people close to developments in EU legislation, EU guidance and standards.

The judgment in the Centre hospitalier universitaire de Besançon v Thomas Dutrueux, Caisse primaire d'assurance maladie du Jura case that I wrote about earlier has been handed down by the EU Court on 21 December and as expected, the EU Court followed its Advocate General.

Vanaf 15 december 2020 moeten reizigers van 13 jaar of ouder met het vliegtuig of per boot, afkomstig uit een land dat niet op de veilige lijst staat, een negatieve testuitslag tonen bij aankomst in Nederland.

On 10 May, Edith Schippers, the Health Secretary in the Dutch Rutte I Government, which tendered its resignation at the beginning of the month, submitted a Draft Act on Continuity, Mergers and Divestments in the Healthcare Sector to the Dutch Lower House.

On May 26, 2021 the Medical Devices Regulation (MDR) entered into effect after a four-year transitional period.

The Authority for Consumers & Markets ("ACM") has made several suggestions with its new draft Guidance regarding "Well-functioning markets for healthcare IT" ("Draft Guidance IT-Healthcare").

On January 28, 2025, the Dutch Minister Agema of Health, Welfare, and Sport sent a letter to the chairman of the House of Representatives...

The joint study released in March also discusses how the COVID-19 pandemic has exacerbated existing problems by opening new opportunities for illicit trade.

A recent case at the European Court of Justice can have important consequences for imports of accessories and disposables for medical devices, as these may be subject to a customs tariff of 6.5 percent.

EU member states are not under all circumstances allowed to restrict the sale of medical devices to only brick-and-mortar shops that specialise in medical devices.

IPPZ is a company that develops software for health care professionals.

I have been running around a lot lately doing presentations on conferences about medical devices and software, so I though it would be useful to give you a round-up on that subject.

Probiotics are known as "beneficial bacteria" that can be found in, amongst others, dairy products and food supplements.

The healthcare sector is one of the NMa's focus industries, which means it is subject to closer investigation.