FDA finalizes Guidance for Electronic Informed Consent

December 2016 – The U.S. Food and Drug Administration (FDA) finalized its guidance intended for institutional review boards (IRBs), investigators, and sponsors engaged in (or responsible for) oversight of human subject research under the Department of Health and Human...

China closes cancer research gap: U.S. shoots for the moon

America prides itself as a leader in technological innovation and medical research. Home to some of the largest and well respected cancer centers in the world, the U.S. has stood as the epicenter for cancer research for several decades. If the U.S. wishes to retain...

Experienced project manager joins Pearl Pathways

Pearl Pathways is pleased to announce the hiring of Shawn Knopp, PhD as an Advisor serving medical device and biopharmaceutical life science companies. Knopp brings to Pearl Pathways over 15 years of experience in multi-disciplinary life science roles including...