This lecture-based, 3-hour live webinar course covers 21 CFR Parts 210, 211, and 600. Topics include the current Good Manufacturing Practices (cGMPs), regulatory compliance, and maintaining a culture of quality …
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 …
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 …
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 …
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 …
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 …
