Regulatory Affairs - CPS
2026-2027
44 courses
- RGA 1010U.S. Regulatory Systems and Agencies
- RGA 1050Regulatory Policy Development
- RGA 1080Pharmaceutical Regulatory Affairs
- RGA 3000Introduction to Safety Science
- RGA 3300Strategic Planning and Project Management for Regulatory Affairs
- RGA 6105Introduction to Regulatory Compliance and Practice
- RGA 6150Regulatory Strategy for Product Development and Life-Cycle Management
- RGA 6208Introduction to Safety Sciences
- RGA 6238Human Experimentation Methodological Issues Fundamentals
- RGA 6285Validation and Auditing of Clinical Trial Information
- RGA 6290Clinical Trial Design Optimization and Problem Solving
- RGA 6295Managing International Clinical Trials
- RGA 6308Pharmaceutical and Medical Device Law: Topics and Cases
- RGA 6350Legal Issues in International Food, Drug, and Medical Device Regulation
- RGA 6400Medical Device Product Development and Process Validation
- RGA 6415Fundamentals of CMC Regulations and Methods
- RGA 6435Medical Device Cybersecurity and Digital Health
- RGA 6440Advanced Topics in Advertising and Promotion of Drugs and Medical Devices
- RGA 6450Financing and Reimbursement in Biomedical Product Development
- RGA 6465Nonclinical Regulations in Biomedical Product Commercialization
- RGA 6475Strategic Planning and Project Management for Regulatory Affairs
- RGA 6480Real-World Evidence and Patient-Reported Outcomes in Regulatory Decision Making
- RGA 6490Emerging Trends and Challenges in Regulatory Affairs
- RGA 6500Biomedical Product Development: Regulatory Affairs in a Market-Based Setting
- RGA 6600Introduction to Food and Drug Administration Pharmaceutical Regulation
- RGA 6610Introduction to Food and Drug Administration Medical Device Regulation
- RGA 6620Medical Device Development: A Regulatory Overview
- RGA 6630Medical Device Quality Management System: Principles and Applications
- RGA 6640Risk Management: Compliance and Processes
- RGA 6650Medical Device Product Development in Canada
- RGA 6660Therapeutic Product Development: A Regulatory Overview
- RGA 6670Global Impact of Electronic Common Technical Document (eCTD) Submissions
- RGA 6675Therapeutic Product Development in Canada
- RGA 6680Project Management in Early Drug Discovery and Development
- RGA 6685European Medical Device Regulations
- RGA 6690Global In Vitro Diagnostic Regulations and Submissions
- RGA 6962Elective
- RGA 6980Capstone: Practical Applications in Global Regulatory Affairs
- RGA 7100Regulatory Frameworks for Biomedical Product Development
- RGA 7110Biomedical Product Post-Market Regulatory Strategy
- RGA 7120Multi-Stakeholder Perspectives in Biomedical Product Access
- RGA 7130Research Methodologies in Regulatory Affairs
- RGA 7962Elective
- RGA 7983Topics
No courses found.