by Waylon Wright | Jun 27, 2017
Pearl Pathways proudly announces the hiring of Patti Connolly, M.S. as Director of Clinical Services. Connolly brings over 30 years of experience in medical research across academic and industry settings, with 10 years dedicated directly to product development,...
by Waylon Wright | Jun 22, 2017
The commissioner of US Food and Drug Administration (FDA), Scot Gottlieb, recently announced an upcoming pilot program, which would create a third-party certification program. The program would be utilized for lower-risk digital health products allowing them to be...
by Waylon Wright | Jun 9, 2017
The U.S. Food & Drug Administration (FDA) announced in a letter on June 2nd its intention to extend the compliance dates for the unique device identification (UDI) system requirements for low-risk devices. Such devices include certain Class I and unclassified...
by Waylon Wright | May 25, 2017
Pearl Pathways is pleased to announce the hiring of Masheka Fuqua as a Clinical Research Associate (CRA) serving biopharmaceutical, medical device, and diagnostics companies. Fuqua brings over a decade of clinical research experience to Pearl Pathways, including the...
by Waylon Wright | May 8, 2017
The Indiana Medical Device Manufacturers Council (IMDMC) is hosting a workshop on May 17, 2017 designed to provide someone new to the medical device industry a background in FDA regulation and to hone the skills of more experienced practitioners. This program has been...
