Curious about the most important things to know BEFORE starting a GLP preclinical study? Now would be the perfect time to attend a webinar! The team at GCMI is excited to announce that we will be hosting a series of webinars starting next week. 


Our first webinar focuses on good laboratory practice (GLP) preclinical studies, which are an essential component to medical product development and regulatory submissions. They are highly rigorous, are conducted in compliance with a legally bound code of federal regulations (21 CFR Part 58) and should be conducted by qualified scientists and staff of an accredited contract research organization (CRO). Ensure you are getting your GLP preclinical study and the resulting data right the first time, by attending this webinar.


Join GCMI’s Preclinical Program Director Evan Goldberg Ph.D. and Senior Program Manager Michael Sweet for a 30 minute webinar on April 16 at 11:00 a.m. intended to help attendees be well prepared BEFORE you start a preclinical GLP study.