We're here when you need us! While you can always reach us for questions by phone, twice a week Biotility staff has open office hours on Zoom where we can answer any questions you …
We're here when you need us! While you can always reach us for questions by phone, twice a week Biotility staff has open office hours on Zoom where we can answer any questions you …
In this lecture-based, three-hour live online course, participants learn the core precepts of FDA’s current Good Manufacturing Practices and their direct application to the manufacture and testing of a regulated …
This course provides future or current employees a comprehensive and applied understanding of how regulatory compliance is built into all aspects of a company. Using a blend of hands-on applications and …
This lecture-based, three-hour live webinar covers FDA's current Good Laboratory Practice (cGLP) regulations and how they affect the conduct of nonclinical laboratory safety studies. This course introduces the various elements …
In the early stages of the pharmaceutical drug approval process, it is essential to maximize outcomes of the Pre-Investigational New Drug (IND) meeting with FDA. Understanding how to navigate initial …
Biotility hosts this general information session to provide an overview of the BACE and the BACE administration process for both potential and returning exam sites. This session is offered multiple …
Biotility hosts this general information session to provide an overview of the BACE and the BACE administration process for both potential and returning exam sites. This session is offered multiple …
Current Good Laboratory Practices (cGLP) are federal regulations set in place to ensure investigational new drugs are safe before testing in humans. They are required when conducting preclinical studies to …
Current Good Manufacturing Practices (cGMP) are federal regulations followed by drug manufacturing companies to ensure their products are safe and effective for humans. Educators will learn the core precepts of …
