by Michele Taylor | Jan 7, 2016
Pearl Pathways is excited to announce its’ participation in the Purdue Economic Gardening Program. The Economic Gardening program is managed by the Purdue Center for Regional Development with funding provided from a gift from the Lilly Endowment Inc. The Purdue...
by Michele Taylor | Jan 6, 2016
According to Zachary Brennan of Regulatory Affairs Professionals Society (RAPS), at the recent December FDA/CMS Summit in Washington, DC, Janet Woodcock, Director of FDA’s Center for Drug Evaluation and Research (CDER) spoke of 2015 accomplishments and gave a look...
by Michele Taylor | Jan 5, 2016
Michael Mezher of Regulatory Affairs Professionals Society (RAPS), recently published an article about the European Medicines Agency (EMA) and its Adaptive Pathways Pilot. The Adaptive Pathways Pilot helps speed up patient access to medicines otherwise not...
by Michele Taylor | Jan 4, 2016
According to Emily Wasserman of Fierce Medical Devices, “FDA is calling for more oversight of lab-developed tests (LDTs)”. In a recent congressional hearing, FDA reviewed 20 case studies where certain LDTs “may have caused or have caused” harm to patients. With this...
by Michele Taylor | Dec 29, 2015
On March 10-11, 2016, the Asia Pacific Device Summit will be held in San Francisco, CA. This event will bring together medical device experts from Asia and the US. Click here for more information. Register for the event through Brandwood Biomedical, Pearl Pathways’...