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 …
BioFlorida Spring Life Sciences Virtual Career Fair Friday, March 25, 2022 1:00 pm - 3:00 pm Meet with life sciences employers across the state to discuss open positions …
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 …
Corrective Action Preventive Action (CAPA) is a process used by biomanufacturing companies to investigate, solve, and prevent problems with the goal of minimizing mishaps. This course will outline the CAPA …
Good Documentation Practices (GDP) are regulatory guidelines that help drug manufacturing companies maintain a system of controlled documents. GDP ensure proper recording, reporting, and archiving of everything involved in the …
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 …
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 …
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 …
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 …