News, views and contacts from the global Medical industry
23 May 2017
Industry News

med fusion introduces EGFR liquid biopsy service with Roche’s mutation test
US-based laboratory diagnostics provider med fusion has introduced a new plasma-based epidermal growth factor receptor (EGFR) liquid biopsy service, which is integrated with Swiss healthcare firm Roche’s cobas EGFR mutation test v2.

Baxter upgrades AK 98 hemodialysis system for broader treatment
US-based healthcare firm Baxter International has introduced the upgraded version of its AK 98 hemodialysis (HD) system to offer more treatment options.

Masimo launches Root patient monitoring with EWS
US-based monitoring technologies developer Masimo has launched its Root patient monitoring and connectivity hub with the early warning score (EWS).

Robocath closes new round of €4.7m financing for new robotic platform
Medical robotics developer Robocath has raised €4.7m through a new round of fundraising to market its latest robotic platform called R-one for cardiovascular indications.

Press Releases

NSF's Global Vice-President Martin Lush to Open 2nd PDA Europe Annual Meeting with Keynote Presentation
NSF International's pharma biotech team has announced it will be present at the 2nd PDA Europe Annual Meeting in Berlin.

maxon motor Magazine Discusses the World of Drive Technology
Precision drive systems can be found in the home, in vehicles, and at work, making our lives simpler and safer.

Formacoat to Showcase Products at MIXiii-BIOMED, Tel Aviv
Formacoat has announced it will be present at the MIXiii-BIOMED event in Tel Aviv, Israel.

Greiner Bio-One Presents New MiniCollect® Complete tube
Following a successful launch of the new capillary blood collection system last autumn, Greiner Bio-One now presents the new MiniCollect® Complete tube as the ideal complement to its innovative system.

Orphan Drug Act 1983 and Rare Diseases
The 21st Century Cures Act stemmed from a political spotlight on two girls that could not get treatment for their rare diseases, as presented by Senator Upton in his opening statement at the Legislative Hearing on 21st Century Cures Act.

White Papers

Five Key Processes for GMP Deviation Investigation
When things go wrong, there are five non-negotiable processes that should be defined on your deviation investigation standards of practice (SOP): immediate engagement, gemba, triaging using...

Are You Ready for UDI?
In an effort to improve the quality of information in medical device adverse event reporting, reduce recalls and improve patient safety, in 2007 the United States Congress passed...

New EU Medical Device Regulation Adopted
This year has brought significant changes to the regulatory landscape across Europe, following the publication of the new European medical device regulation (MDR) and in-vitro...

Are You Facing a Complexity Crisis?
In this whitepaper, Martin Lush discusses the issue of over-complexity in the pharmaceutical...

What is Micro-Molding?
There seems to be a lot of talk these days about micro-molding. This reflects the increased interest from designers and manufacturers in producing and procuring high precision,...

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