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Clin Research Regulations
|Course||Course Title||Class||Lab/ Shop||Clinical/ Co-op||Credit|
|CTR 115||Clin Research Regulations||3||0||0||3|
|Effective Term: Spring 2001|
This course covers the range of national and international regulations governing the development of drugs, diagnostics, medical devices, and biologics. Topics include a review of the regulatory agencies, guidelines for regulatory application, required documentation, and preparation for compliance audits. Upon completion, students should be able to demonstrate a basic understanding of regulatory processes associated with clinical research and describe effective means of compliance.
- : Comprehensive Articulation Agreement - This course is recommended for students transferring to a four-year university.
- : Local Requirement
- : Instructional Service Agreement
- : Universal General Education Transfer Component (UGETC)
- : Global Distinction
- : Requisite(s)
This Course can be found in these Programs of Study
- Nanotechnology - Clinical Trials Research - Certificate (Day)