Prepare with RAPS : RAC-GS exam braindumps as your best preparation materials

Updated: Sep 09, 2026

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Compared to other resources, the following are the reasons for choosing the RAPS RAC-GS exam dumps for the prep of the exam. The questions are prepared by experts who have vast experience in writing the RAC exams. Therefore, you will get the most authentic queries and answers. The material provided is arranged logically, so It is easy to get an overview of the entire paper. Trial questions are also available on this website. There are multiple-choice and essay-based questions that will test your understanding of the concepts. You can download PDF files of the practice exams of the RAC-GS from the website or mobile app. The questions are authentic and were taken from the real-time exams. Therefore, there is no chance of getting any type of queries that are not used in the actual exam. Guarantee of passing the certification exam. It is our refund policy if individuals fail in the RAC-GS Certification Exam they can request to claim a refund of the money they paid.

Introduction to the RAPS RAC-GS Certification Exam?

Regulatory Affairs Certification (RAC) Global Scope is simply called RAC-GS Certification Exam. This Certification Exam is designed by the RAPS to test the candidate's knowledge, skills, and abilities in Regulatory Affairs (R&D), Health Science (Pharmaceutical), Biotechnology, medicinal Device, and Public Health, to meet the requirements of Regulatory Affairs Professionals and other stakeholders. RAC-GS exam dumps can help you get your certification easily. The RAC-GS Certification Exam is also intended for use by educational and training institutions offering R&D programs and academic degrees related to regulatory affairs, health science, biotechnology, medical device, and public health. Investors, people in financial services, business analysts, and consultants are also eligible to take this exam. Labeling is granted to individuals who pass the exam. The candidates must then pass the RAC-GS Certification Exam as well as the RAPS RAC-GS Certification Exam.

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Passing Score, Duration, No of question, languages, Format of the RAPS RAC-GS Certification Exam

RAC-GS exam dumps elaborated the detailed info about the exam. The overview of the info about Passing Score, Duration & Question for the RAPS RAC-GS Certification is given below:

  • No. of questions: 100
  • Exam Format: MCQs
  • Languages: English
  • Time Duration: 120 Minutes
  • Passing score: 65%

RAPS RAC-GS Exam Overview:

Certification Vendor:Regulatory Affairs Professionals Society (RAPS)
Exam Name:Regulatory Affairs Certification (RAC) Global Scope Exam
Exam Number:RAC-GS
Exam Duration:210 minutes
Available Languages:English
Real Exam Qty:150-180
Certificate Validity Period:3 years
Exam Format:Multiple Choice, Recall, Computer-Based, Application, Analysis
Related Certifications:RAC-Drugs
RAC-Devices
Passing Score:70%
Exam Price:$605 (RAPS Member), $760 (Non-Member) - 2026 rates
Recommended Training:RAPS Online University
RAPS Fundamentals Textbooks
Exam Registration:RAPS Official Application
Pearson VUE Scheduling
Sample Questions:RAPS RAC-GS Sample Questions
Exam Way:Computer-based testing at Pearson VUE centers or online remote proctoring
Pre Condition:Bachelor's degree + 3 years regulatory experience; Master's + 2 years; Doctorate + 1 year; RAPS membership recommended
Official Syllabus URL:https://www.raps.org/certifications/rac

RAPS RAC-GS Exam Syllabus Topics:

SectionWeightObjectives
Topic 1: Regulatory Submissions & Approval20%- Review Process & Interactions
  • 1. Regulatory Authority Interactions
    • 2. Deficiencies & Response Management
      - Global Dossiers & Submission Formats
      • 1. CTD/eCTD Structure
        • 2. National & Regional Application Routes
          Topic 2: Product Development & Lifecycle Management25%- Chemistry, Manufacturing & Controls
          • 1. Quality Systems & Documentation
            • 2. GMP Requirements
              - Clinical Research & Trials
              • 1. GCP Compliance
                • 2. Global Clinical Submissions
                  Topic 3: Global Regulatory Environment & Strategy35%- International Regulatory Frameworks
                  • 1. Regional Regulatory Systems
                    • 2. ICH, WHO, IMDRF, ISO Guidelines
                      - Regulatory Strategy & Planning
                      • 1. Global Market Access Strategy
                        • 2. Regulatory Intelligence & Risk Management
                          Topic 4: Post-Market Compliance & Surveillance20%- Labeling, Advertising & Changes
                          • 1. Global Labeling Rules
                            • 2. Post-Approval Changes & Variations
                              - Pharmacovigilance & Adverse Events
                              • 1. Global Reporting Requirements
                                • 2. Risk Management Plans

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