This webinar will provide an overview of safety assessment of metabolites in drug development. The speaker will discuss relevant guidance documents and will describe important considerations for the safety assessment of drug metabolites, including type of studies required and timing of submission to
ACT ToxChats (podcasts) is excited to preview the upcoming ACT webinar titled, “Immunological Assessments of Viral Vectors Expressing Multiple Cytokine Transgenes in Nonclinical Studies,” which is scheduled for September 25 at 11:00 AM ET.
The purpose of this webinar is to provide early career professionals with a general understanding of the design of Acute/Dose Range Finding (DRF) studies and identification/selection of a high dose level.
You are invited to participate in an ACT free educational webinar, A Regulatory and Industry Perspective on the Introduction and Application of GLP Regulations: What They Are, Why They Matter, and How They Apply to Toxicology Studies on Wednesday, May 29, 2019 at 11:00 AM ET.