by Waylon Wright | Nov 15, 2016
The China Food and Drug Administration announced that manufacturers will be able to request priority review and approval of Class II (limited to imported application) and Class III (both domestic and imported application) devices exported to China beginning January 1,...
by Waylon Wright | Nov 15, 2016
On Thursday, November 17th, Purdue University’s professor of Medicinal Chemistry, Dr. Stephen R. Byrn, will host a free webinar exclusive for members of the Indiana Regulatory Affairs Professionals Society (RAPS) Chapter. Members may register for the webinar...
by Waylon Wright | Nov 9, 2016
On Tuesday, November 15th, learn about some of the best practices being adopted by leading medical device companies and startups alike. This webinar will focus on the first ‘observational’ phase, which involves identifying unmet, unarticulated, and underserved...
by Waylon Wright | Nov 9, 2016
Artificial Intelligence (‘AI’) has been in the media spotlight for various reasons as of late. A debate is underway concerning the integration of AI in our businesses, phones, art, and nearly everything else one can imagine. Companies within the healthcare industry...
by Waylon Wright | Nov 7, 2016
Pearl Pathways is excited to announce the hiring of Michele Taylor as a regulatory compliance analyst. Taylor will help the Pearl team serve medical device and biopharmaceutical life science companies. Taylor brings 12 years of experience in Project Management in Life...
