DataRevive USA LLC

ELIQUENT will be at BIO Asia-Taiwan (July 25-28). Meet the team at booth #M928 - or schedule a meeting via the link: https://lnkd.in/ednBz4DK

Japan's domestic pharmaceutical market reached a record-breaking high of 11.3 trillion yen in 2023. As one of the world’s leading economies, Japan offers life science organizations the unique opportunity to expand their market potential within a supportive regulatory environment. Read Eliquent Japan, Inc Japan's blog post examining the unprecedented growth of this thriving market and learn how our team brings value to life science innovators entering the Japanese market. https://lnkd.in/eP356v-f

ELIQUENT Expert, Michele Dougherty, examines the FDA's recent update to a draft guidance addressing studies supporting a biological product's interchangeability with reference products. Read Michele's analysis at https://lnkd.in/egv85Ezj

ELIQUENT welcomes Shaun Stapleton to the team - Shaun is a senior regulatory affairs and drug development professional with extensive international experience in the pharma, biotech and consulting environments. Learn more about Sean at https://lnkd.in/eVYVD7ri

Members of the ELIQUENT team will be at the annual BIO International Meeting next week in San Diego. Schedule on-site meetings with the team by following the QR codes in our post or via these links: Global Regulatory Affairs: https://qrco.de/bf6WZ2; Japan Regulatory Affairs: https://qrco.de/bf6WTq; and Quality & Compliance: https://qrco.de/bf6WaI. Learn more about ELIQUENT’s comprehensive capabilities at ELIQUENT.com

ELIQUENT Expert - Ziqi Zhang - addresses the pivotal role IND maintenance plays in clinical trials. Read Ziqi's white paper examining the impact on patient safety and data integrity at ELIQUENT.com https://lnkd.in/epmjSrus

Members of the ELIQUENT team - Christine Scheve, MSBME, Heidi H., Mikio Ishizawa, and Igor Ilievski MD MBA - will be in San Diego the week of June 3rd for the annual Biotechnology Innovation Organization International Convention. Schedule a meeting with the team via [email protected]

ELIQUENT Expert, Maura Norden, will join Heather Pearson and Danielle Sloane of Bass, Berry & Sims, for a webinar on May 22nd addressing FDA's final rule outlining the regulation of laboratory-developed tests (LDTs). To register for the webinar, visit https://lnkd.in/e8bME7Pg and to learn more about ELIQUENT’s LDT capabilities, visit eliquent.com

ELIQUENT Expert - Chris Leptak, MD, PhD - will be on faculty for a course addressing biomarkers in clinical studies at the Annual Scientific Meeting for the American Spinal Injury Association (ASIA).

SPEAKER SPOTLIGHT: ELIQUENT Experts Kalah Auchincloss and Janet Michener Whipple will speak at today's Food and Drug Law Institute (FDLI) Annual Conference. See the meeting agenda and speaker profiles at https://lnkd.in/dF7sa2Xe