Below is a copy from the FDA webpage on Innovation Pathway. Innovation Pathway Background on CDRH Innovation On Feb. 8, 2011, the FDA’s Center for Devices and Radiological Health launched its Innovation Initiative, which proposed actions the agency could take
Top 10 Medical Cities Now & Future
In an article from MedCityNews.com on Dec 12, 2011 has an interesting take on a top 10 medical city list. They look at it from the traditional lists to looking in the future with their fortune telling crystal ball. For
GHTF to morph into Int’l Med Dvc Regulators’ Forum (IMDRF)
The GHTF has been around for almost 20 years and is in the process of disbanding to become a more Regultor focused group called the International Medical Device Regulators’ Forum (IMDRF). In the Eucomed 18 Nov 2011 newsletter article they
FDA Extends Comment Period on 510(k) Guidance
On November 8, 2011 FDA issued a notice in the Federal Register extending the public comment period for the draft Guidance Document “510(k) Device Modifications: Deciding When to Submit a 510(k) for a Change to an Existing Device” from October
Tracking Vital Signs, Without the Wires
In the New York Times on Sept 3, 2011 – The article starts ‘CONFINED to their hospital beds, patients can only fantasize about stripping off all the wires that connect them to monitors and bolting for the door…’