RGA courses
43 courses · Northeastern University · Fall 2026
- RGA 5101 — Therapeutic Product Development: A Regulatory Overview1 section
- RGA 5202 — Medical Device Development: A Regulatory Overview1 section
- RGA 5212 — Introduction to Safety Sciences1 section
- RGA 5463 — Regulatory Strategy for Product Development and Life-Cycle Management1 section
- RGA 6000 — Introduction to Food and Drug Administration (FDA) Pharmaceutical Regulation1 section
- RGA 6001 — Introduction to Food and Drug Administration (FDA) Medical Device Regulation1 section
- RGA 6002 — Introduction to Regulatory Compliance and Practice1 section
- RGA 6101 — Therapeutic Product Development: A Regulatory Overview1 section
- RGA 6202 — Medical Device Development: A Regulatory Overview1 section
- RGA 6203 — Pharmaceutical and Medical Device Law: Topics and Cases1 section
- RGA 6204 — Legal Issues in International Food, Drug, and Medical Device Regulation1 section
- RGA 6205 — Emerging Trends and Issues in the Medical Device Industry1 section
- RGA 6207 — Global Impact of Electronic Common Technical Document (eCTD) Submissions1 section
- RGA 6210 — Strategic Planning and Project Management for Regulatory Affairs1 section
- RGA 6212 — Introduction to Safety Sciences1 section
- RGA 6215 — Project Management in Early Drug Discovery and Development1 section
- RGA 6217 — Biomedical Product Development: From Biotech to Boardroom to Market1 section
- RGA 6219 — Advanced Topics in Advertising and Promotion of Drugs and Medical Devices1 section
- RGA 6221 — European Union Compliance Process and Regulatory Affairs1 section
- RGA 6222 — European Medical Device Regulations1 section
- RGA 6223 — Introduction to Australian, Asian, and Latin American Regulatory Affairs1 section
- RGA 6224 — Regulation of Biomedical Product Commercialization by Health Canada1 section
- RGA 6228 — Managing International Clinical Trials1 section
- RGA 6233 — Application of Quality System Regulation in Medical Device Design and Manufacturing1 section
- RGA 6234 — Risk Management: Compliance and Processes1 section
- RGA 6235 — Emerging Product Categories in the Regulation of Drugs and Biologics1 section
- RGA 6243 — Medical Device Product Development in Canada1 section
- RGA 6244 — Therapeutic Product Development in Canada1 section
- RGA 6250 — Financing and Reimbursement in Biomedical Product Development1 section
- RGA 6275 — Product Development and Process Validation1 section
- RGA 6300 — Practical Applications in Global Regulatory Affairs1 section
- RGA 6370 — Advanced Regulatory Writing: Medical Device Submissions1 section
- RGA 6380 — Advanced Regulatory Writing: New Drug Applications1 section
- RGA 6405 — Nonclinical Regulations in Biomedical Product Commercialization1 section
- RGA 6410 — Fundamentals of CMC Regulations and Methods1 section
- RGA 6420 — Global IVD Regulations and Submissions1 section
- RGA 6432 — Real-World Evidence in Biomedical Research1 section
- RGA 6461 — Cybersecurity and Regulation of Digital Health Technologies by the FDA1 section
- RGA 6463 — Regulatory Strategy for Product Development and Life-Cycle Management1 section
- RGA 6962 — Elective1 section
- RGA 6980 — Capstone: Practical Applications in Global Regulatory Affairs1 section
- RGA 7962 — Elective1 section
- RGA 7983 — Topics1 section
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