778027 - Teaching CGMP as a Workplace Skill
Course Description
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 CGMP, and the FDA regulatory guidelines required for companies who manufacture drugs, drug products, and medical devices. The course will also review strategies and classroom activities to support educators as they integrate CGMP concepts into their classrooms to prepare students for future success in bioscience industry careers.

Course Fee
$250 per participant
Duration
Participants have 90 days following enrollment in which to complete the course.
Course Access
To access your course after enrollment, please click the link below.
Click the blue “Log in to Continuing Education” button and enter your login credentials (be sure to use the same third-party credentials you entered during enrollment). You should then see your course on the UF e-Learning dashboard or by clicking Courses>All Courses.
Please note, it is common practice to enroll in multiple courses or sections in order to access all online content relevant to your program. However, you will only create one UF account once (during your first enrollment).
Contact Us
If you have questions or need assistance, please contact Jenny Hughes
Phone: 386.518.2118
Email: biotility@research.ufl.edu
Learner Outcomes
- Understand how current Good Manufacturing Practices (CGMP) support the production of safe and efficacious drugs intended for use in humans
- Review the historical events that led to the establishment of CGMP
- Develop familiarity with CGMP regulations and how they apply to the process of pharmaceutical and biopharmaceutical drug production
- Appreciate the impact of CGMP regulations on departmental roles and company culture within the pharmaceutical and biopharmaceutical industry
- Communicate career opportunities within the pharmaceutical, biopharmaceutical, and biotechnology industries
- Apply enhanced understanding of CGMP through various activities and best practices