Gretchen Bowker, COO and Head of Quality of Pearl IRB, will share insights during an Indiana Health Industry Forum (IHIF) lunch event on Tuesday, December 19, 2017. The lunch event, “Perspectives on the FDA” is part of IHIF’s recurring Life Sciences...
The United States Food and Drug Administration (FDA) released a new draft guidance as part of its stated commitment to assist sponsors and expedite drug development for rare pediatric diseases, Outsourcing-Pharma.com reports. FDA collaborated with the European...
Join Diana Caldwell, President and CEO of Pearl IRB, this Friday, December 1, 2017 at Purdue Foundry as she discusses “The Power of LinkedIn for Life Science Professionals.” Foundry Grounds occurs each Friday and involves conversations, presentations &...
Gretchen Bowker, COO and Head of Quality at Pearl IRB, will discuss the regulatory approval process at the VisionTech Partners meeting on Thursday, November 30, 2017. The event, “Don’t Wine about FDA – Regulatory 101 with Pearl Pathways,” is...
It should come as no surprise that the volume and diversity of clinical trial data is expected to rapidly increase over the next few years. The proliferation of mobile health tech, real world evidence (RWE), electronic data capture (EDC) systems, etc. in the clinical...
