by Avery Zimmerman | Mar 7, 2023 | Blog
The CDISC Standard for the Exchange of Nonclinical Data (SEND) requirements for US Investigation New Drug Applications (INDs), New Drug Applications (NDAs), and Biologics License Applications (BLAs) requirements, designed to improve the ease of nonclinical data review...
by Avery Zimmerman | Feb 10, 2023 | Blog
The FDA recently proposed to replace its current annual reporting requirements for Investigational New Drug (IND) applications with Development Safety Update Reports (DSURs). What Does the FDA’s Proposed Change Mean? Under 21 CFR 312.33, FDA requires Sponsors with an...
by Avery Zimmerman | Feb 7, 2023 | News
CANTON, Mich. (2/7/2023) – MMS Holdings (MMS) – an award-winning, data-focused contract research organization (CRO) – announces the expansion of its leadership team with the appointment of Chris Schoonmaker as Chief Operating Officer and Ashu Tandon as Chief...
by Avery Zimmerman | Feb 6, 2023 | Blog
Project Renewal is an initiative established by the FDA to reassess outdated oncology drug products and modernize them. The Oncology Center of Excellence (OCE) recently approved a labeling update for Genentech’s capecitabine tablet, known as Xeloda. In this labeling...
by Avery Zimmerman | Feb 2, 2023 | Blog
New recommendations for IRB review, informed consent and expanded access policies. FDA recently announced the availability of a revised draft Guidance for industry on expanded access (EA) to investigational new drugs (INDs) for treatment use, which consists of...
