By Stewart Eisenhart, Emergo Group
Emergo Group periodically conducts medical device industry research. A few of the studies we have conducted are shown below. You may download these in PDF format by clicking the links.
The Medical Device Business Journal — Medical Device News & Articles | MassDevice
By Stewart Eisenhart, Emergo Group
Emergo Group periodically conducts medical device industry research. A few of the studies we have conducted are shown below. You may download these in PDF format by clicking the links.
By Stewart Eisenhart, Emergo Group
Germany’s medical technology industry has seen sales rates grow by more than five percent according to a survey by the German Medical Technology Association (BVMed).
By Stewart Eisenhart, Emergo Group
European medical technology trade association Eucomed has issued a new position paper advocating six major changes to how the European Union regulates medical devices.
By Stewart Eisenhart, Emergo Group
The Drug Controller General (India) (DCGI) has announced plans to prescreen registration applications for medical devices and pharmaceutical products upon receipt beginning December 1, 2011.
By Stewart Eisenhart, Emergo Group
The US Food and Drug Administration is seeking further comment on its proposed approach for evaluating highly multiplexed microbiology and medical countermeasure diagnostic devices.
By Stewart Eisenhart, Emergo Group
A new report examining European in vitro diagnostic (IVD) market performance in 2010 sees flat or negative growth across most major EU member states due to cost containment measures and worsening economic conditions.
By Stewart Eisenhart, Emergo Group
As it transforms into a new organization, the Global Harmonization Task Force (GHTF) continues to issue guidances likely to influence major medical device regulators worldwide.
Say hello to MassDevice +3Blogs, a bite-sized view of the top three med-tech blogs of the week. This latest feature of MassDevice.com’s coverage highlights our three favorite blogs of the week to make sure you’re up to date on the headlines that continue to shape the medical device industry.
If you read nothing else this weekend, make sure you’re still in the know with MassDevice +3Blogs.
By Stewart Eisenhart, Emergo Group
Two versions of a draft law amending regulations of pharmaceutical and medical technology products in France have been adopted by the French National Assembly and Senate.
By Stewart Eisenhart, Emergo Group
The Global Harmonization Task Force (GHTF) will evolve into the International Medical Device Regulators’ Forum (IMDRF), with the new organization’s inaugural meeting set to take place in Singapore in early 2012.
Say hello to MassDevice +3Blogs, a bite-sized view of the top three med-tech blogs of the week. This latest feature of MassDevice.com’s coverage highlights our three favorite blogs of the week to make sure you’re up to date on the headlines that continue to shape the medical device industry.
If you read nothing else this weekend, make sure you’re still in the know with MassDevice +3Blogs.