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Updated: Jul 18, 2026
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Why it is important to take the RAPS RAC-GS Certification Exam?
In this era of Globalization and the need for global harmonization in various domains such as Health, Financial Services, medicinal Devices, Pharmaceuticals, Public Health, and Bio-Technology, it has become important for Regulatory Affairs Professionals to have the RAC-GS Certification Exam and show their knowledge, skills, and abilities in various areas of Regulatory Affairs. This Certification Exam will enable Regulatory Affairs Professionals to identify themselves and their professional skills in various areas of regulatory affairs. The RAC-GS exam dumps are a great tool to help you get certified for this exam. Electronic slideshows or audiovisual materials are also needed from candidates. Embedded music is prohibited. Candidates must submit an original and unmodified picture of themselves with their official credentials, a copy of their passport, and a brief biography.
The Process to prepare for the RAPS RAC-GS Certification Exam is elaborated below:
The process to prepare for the RAPS RAC-GS Certification exam consists of various activities. Here is a brief overview of the steps to prepare for a RAPS RAC-GS Certification exam:
First, you need to go through the RAPS RAC-GS Certification Exam details and prepare well for it. Pivotal RAPs RAC-GS Certification Exam details are provided by the RAPS.
Once you are done with the practice, you need to revise the topics and concepts that you have not understood properly.
After reading the exam content, start preparing by doing mock tests. You can also get ideas for prep from RAC-GS exam dumps. This will help you to identify your weak areas and get the right idea about the questions that will be asked in the exam.
Practice hard for the test, as you will have only four hours to complete the exam.
RAPS RAC-GS Exam Overview:
| Certification Vendor: | Regulatory Affairs Professionals Society (RAPS) |
| Exam Name: | Regulatory Affairs Certification (RAC) Global Scope |
| Exam Number: | RAC-GS |
| Related Certifications: | RAC-Drugs RAC-Devices |
| Passing Score: | Scaled pass score set by RAPS (official pass mark not publicly published) |
| Real Exam Qty: | Approx. 180 (divided into two parts) |
| Exam Price: | Fees vary by testing window and membership status (typically higher for non-members) |
| Exam Duration: | Approx. 210 (3.5 hours) |
| Exam Format: | Multiple choice, Computer-based |
| Available Languages: | English |
| Sample Questions: | RAPS RAC-GS Sample Questions |
| Exam Way: | Computer-based testing at Pearson VUE centers or online proctored |
| Pre Condition: | Typically at least three years of regulatory affairs or related professional experience; specific prerequisites are determined by RAPS |
| Official Syllabus URL: | https://www.raps.org/certifications/rac/what-is-the-rac |
Topics covered by the RAPS RAC-GS Certification Exam:
RAC-GS exam dumps will cover the following topics of the RAC-GS Certification Exam:
- Bio-Technology: 20%
- Health Science: 10%
- Pharmaceuticals: 25%
- Public Health: 10%
- Medical Devices: 35%
RAPS RAC-GS Exam Syllabus Topics:
| Section | Objectives |
|---|---|
| Topic 1: Global Regulatory Environment | - Global harmonization standards (e.g., ICH, WHO) - International regulatory frameworks |
| Topic 2: Product Lifecycle Management | - Pre-market requirements - Post-market compliance and pharmacovigilance |
| Topic 3: Regulatory Strategy and Submissions | - Regulatory submission pathways - Strategic planning for global filings |
| Topic 4: Country-Specific Regulations | - US regulatory requirements - EU regulatory requirements |
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