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Complete Course Directory

Courses are composed of several topical lessons featuring interactive exercises, detailed explanatory text, engaging graphics, as well as hyperlinks to additional reference material and resources. A short quiz at the end of each lesson measures your incremental learning and an all-inclusive final exam measures your overall comprehension of the course's subject. Navigate through course lessons at your own pace and schedule.

An array of individual courses, focused on regulatory and business topics are available, from general knowledge to product- and region-specific topics. Individual courses are the ideal way to address any knowledge gaps or enhance understanding of a specific area for yourself or your staff.


Group Rates

Group Rates AvailableTo learn more about group rates, simply email raps@raps.org and let us assist you in creating a package that meets the training needs of your team or organization.


Certificate Programs


Bundles

Course Listing

Medical Devices Certificate Program course - Purchase individually or as part of the Regulatory Affairs Certificate: Medical Devices
Pharmaceuticals Certificate Program course - Purchase individually or as part of the Regulatory Affairs Certificate: Pharmaceuticals

Clinical
Good Clinical Practice (GCP)  Medical Devices Certificate Program course Pharmaceuticals Certificate Program course Register
Understanding and Managing the US Clinical Trial Process Medical Devices Certificate Program course Pharmaceuticals Certificate Program course Register

Essentials
Effective Communication and Negotiation Medical Devices Certificate Program course Pharmaceuticals Certificate Program course Register
Ethics Medical Devices Certificate Program course Pharmaceuticals Certificate Program course Register
FDA Law and Regulation Medical Devices Certificate Program course Pharmaceuticals Certificate Program course New! Register
Intermediate Medical Writing: Biologics and Pharmaceuticals Pharmaceuticals Certificate Program course New! Register
Intermediate Medical Writing: Investigational Applications Medical Devices Certificate Program course Pharmaceuticals Certificate Program course New! Register
Intermediate Medical Writing: Medical Devices Medical Devices Certificate Program course New! Register
Introduction to Global Healthcare Product Regulations Medical Devices Certificate Program course Pharmaceuticals Certificate Program course Register
Introductory Medical Writing Medical Devices Certificate Program course Pharmaceuticals Certificate Program course Register
Project Management for Regulatory Professionals Medical Devices Certificate Program course Pharmaceuticals Certificate Program course Register
Regulatory Due Diligence for Product Development  Medical Devices Certificate Program course Pharmaceuticals Certificate Program course New! Register
The Role of the Regulatory Professional Medical Devices Certificate Program course Pharmaceuticals Certificate Program course Register
Supplier Management Regulatory Basics Bundle Pharmaceuticals Certificate Program course New! Register
Supply Chain Controls /online-university/complete-course-directory/supply-chain-controls.aspx Pharmaceuticals Certificate Program course New! Register

Medical Devices
Global Regulatory Strategy for Medical Devices Medical Devices Certificate Program course Register
Medical Devices: Canadian Regulations Medical Devices Certificate Program course Register
Medical Devices: China, Japan, Singapore and South Korea Regulation Overview Medical Devices Certificate Program course New! Register
Medical Devices: Compliance and Audits Medical Devices Certificate Program course Register
Medical Devices: Corrections, Removals and Directed Recalls Medical Devices Certificate Program course New! Register
Medical Devices: Definition and Lifecycle Medical Devices Certificate Program course Register
Medical Devices: EU Regulations Medical Devices Certificate Program course Register
Medical Devices: Postmarket Surveillance Medical Devices Certificate Program course Register
Medical Devices: Risk Management Medical Devices Certificate Program course Register
Medical Devices: US Regulations Medical Devices Certificate Program course Register
Regulation of Combination Products Medical Devices Certificate Program course Pharmaceuticals Certificate Program course Register
Regulation of IVDs in the US Medical Devices Certificate Program course Register

Pharmaceuticals
Chemistry, Manufacturing and Controls (CMC) Pharmaceuticals Certificate Program course New! Register
Global Regulatory Strategy for Pharmaceuticals Pharmaceuticals Certificate Program course Register
Pharmaceuticals: Canadian Regulations Pharmaceuticals Certificate Program course Register
Pharmaceuticals: Compliance and Audits Pharmaceuticals Certificate Program course Register
Pharmaceuticals: Definition & Lifecycle Pharmaceuticals Certificate Program course Register
Pharmaceuticals: EU Regulations Pharmaceuticals Certificate Program course Register
Pharmaceuticals: US Regulations Pharmaceuticals Certificate Program course Register
Pharmacovigilance Pharmaceuticals Certificate Program course Register
Regulation of Combination Products Medical Devices Certificate Program course Pharmaceuticals Certificate Program course Register
Regulation of Dietary Supplements and NHPs Pharmaceuticals Certificate Program course New! Register
Regulation of Generic Drugs in the US Pharmaceuticals Certificate Program course New! Register
Regulation of US and EU Biologics Pharmaceuticals Certificate Program course Register
REMS and RMPs Pharmaceuticals Certificate Program course Register

Quality
Good Laboratory Practice (GLP) Medical Devices Certificate Program course Pharmaceuticals Certificate Program course Register
Good Manufacturing Practice (GMP) Pharmaceuticals Certificate Program course Register
Quality System Regulations (QSRs) Medical Devices Certificate Program course Register

Registration Forms

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"I am glad I could choose courses to customize the information for my own use. The courses were written by knowledgeable instructors who had worked in the field. I found the depth of the information very useful."

– Harry Holden, RA/QA officer