Workforce Continuing Education Course Catalog

Browse the catalog below to see what we offer. New courses added regularly!

If you have questions about the status of a non-degree Workforce Continuing Education class, please contact the staff member listed as the course contact. You can find the course contact by clicking on the title of a course in the catalog below, then clicking on the "more details" tab. You can also email the WCE registrar’s office at [email protected].

Need financial assistance to take a course? See if you qualify for funding through the Workforce Continuing Education Career Pathways Program & Student Resources department

CGMP Overview for Pharmaceuticals
Available Classes
    Section Location Begin Date End Date Instructor Price Seats Available/Total Seats
235735 Face-to-Face Online Instruction 10/09/2020 10/09/2020 G. Smith $70.00 18/20
235747 Face-to-Face Online Instruction 10/23/2020 10/23/2020 G. Smith $70.00 20/20
Description Course Outline Requirements Intended Audience More Details
Intended Audience
Manufacturing Technicians, Team Leaders and Supervisors, Quality Control Personnel, Quality Assurance Personnel, Maintenance/Engineers
An overview of Current Good Manufacturing Practices (CGMP) fundamentals used by pharmaceutical and biomanufacturing companies. CGMP exists to protect the health and safety of patients and consumers which supports the mission of the Food and Drug Administration (FDA). This course equips professionals whose responsibilities depend on operating in CGMP and regulated facilities.
Course Objectives
  1. Define the elements of current Good Manufacturing Practices (CGMP) for biomanufacturing and pharmaceutical production.
  2. Explain how CGMP helps regulated companies comply with the law: Part 21 of the Code of Federal Regulations (21 CFR 211).
  3. Understand the importance of current Good Documentation Practices (CGDP) for pharmaceuticals and Part 11 of the Code of Federal Regulations (Electronic Record Keeping).
  4. Recognize the consequences of failing to comply with CGMP.
Outline of Instruction
  1. The mission of the FDA
  2. The quality assurance role
  3. Personnel and organization
  4. Buildings and facilities
  5. Equipment
  6. Control of components, drug product containers, and closures
  7. Production and process controls
  8. Packaging and labeling
  9. Holding and distribution
  10. Laboratory controls
  11. Records and reports
  12. Return and salvaged drug products
  13. Complaints and recalls
  14. Good Documentation Practices (GDP)
  15. Computer systems (Part 11)
  16. Regulatory enforcement
Contact Hours
Industry Standard, State, or National Certification
CE to CU Articulation
Text and Supplies Needed
Provided by BioNetwork
Clinical Site/Special Facilities
Requirements for Successful Completion of this Course
  1. Attendance 100%
  2. Participation
Accreditation/Special Approval Requirements
Intended Audience
Manufacturing Technicians, Team Leaders and Supervisors, Quality Control Personnel, Quality Assurance Personnel, Maintenance/Engineers
Specific Industry or Business Support Needs
Industry or Job Titles Related to training Outcomes for Employment
  • Manufacturing Technicians
  • Team Leaders and Supervisors
  • Quality Control Personnel
  • Quality Assurance Personnel
  • Maintenance/Engineers
Related Courses
  • Medical Devices, CGMPs and ISO Overview - SEF-414CL
  • Elements of Current Good Manufacturing Practices in Biomanufacturing Processes - SEF-79524
Course Contact Information
Bionetwork Manager