Regulatory Affairs - CPS RGA
24 courses · Northeastern University · Fall 2026
- RGA 6105 — Introduction to Regulatory Compliance and Practice6 sections
- RGA 6150 — Regulatory Strategy for Product Development and Life-Cycle Management5 sections
- RGA 6208 — Introduction to Safety Sciences2 sections
- RGA 6238 — Human Experimentation Methodological Issues Fundamentals2 sections
- RGA 6285 — Validation and Auditing of Clinical Trial Information4 sections
- RGA 6290 — Clinical Trial Design Optimization and Problem Solving3 sections
- RGA 6295 — Managing International Clinical Trials2 sections
- RGA 6308 — Pharmaceutical and Medical Device Law: Topics and Cases3 sections
- RGA 6400 — Medical Device Product Development and Process Validation2 sections
- RGA 6415 — Fundamentals of CMC Regulations and Methods1 section
- RGA 6475 — Strategic Planning and Project Management for Regulatory Affairs1 section
- RGA 6600 — Introduction to Food and Drug Administration Pharmaceutical Regulation3 sections
- RGA 6610 — Introduction to Food and Drug Administration Medical Device Regulation2 sections
- RGA 6620 — Medical Device Development: A Regulatory Overview3 sections
- RGA 6630 — Medical Device Quality Management System: Principles and Applications3 sections
- RGA 6640 — Risk Management: Compliance and Processes2 sections
- RGA 6650 — Medical Device Product Development in Canada1 section
- RGA 6660 — Therapeutic Product Development: A Regulatory Overview3 sections
- RGA 6670 — Global Impact of Electronic Common Technical Document (eCTD) Submissions4 sections
- RGA 6675 — Therapeutic Product Development in Canada2 sections
- RGA 6680 — Project Management in Early Drug Discovery and Development4 sections
- RGA 6685 — European Medical Device Regulations2 sections
- RGA 6690 — Global In Vitro Diagnostic Regulations and Submissions1 section
- RGA 6980 — Capstone: Practical Applications in Global Regulatory Affairs1 section
Spot missing or incorrect course data?