by Charlie Perrecone | May 22, 2013
Stewart Eisenhart, of Massdevice.com, reported that the China Food & Drug Administration (CFDA) is moving forward with improvements to their classification of medical devices process and is simplifying the road to the market for innovative devices. China has a...
by Charlie Perrecone | May 22, 2013
On Thursday, May 16th, Zachary Brennan reported, on in-PharmaTechnologist.com, that the bill H.R. 1919 has advanced passed the US House Energy & Commerce Committee. The bill, written by Rep. Bob Latta promises to further secure the US prescription drug supply...
by Charlie Perrecone | May 16, 2013
In-PharmaTecnologist.com’s Zach Brennan wrote a recent article about Canada’s agreement to strengthen the GMP requirements on active pharmaceutical ingredients (API). Canada is one of the last industrialized countries to extend GMP requirements on APIs but in doing so...
by Charlie Perrecone | May 16, 2013
The St. Vincent Research and Regulatory Affairs will be hosting the 9th Annual St. Vincent Health Research Symposium next month. This daylong event will feature keynote speakers, William Droegemueller, MD, Distinguished Clinical Professor, Obstetrics and Gynecology at...
by Charlie Perrecone | May 16, 2013
In a recent article on massdevice.com, Brad Perriello shares interesting data from Pricewaterhouse Coopers’ (PWC) US Pharmaceutical and Life Sciences Deals Insights Quarterly report Medical device mergers and acquisition deals in the first quarter fell from eight in...
