If you are looking to enhance your regulatory affairs career and want to earn a globally recognized certification, then the RAC-GS Regulatory Affairs Certification (RAC) Global Scope exam is for you. The RAC-GS exam is designed to evaluate your regulatory affairs knowledge and expertise in a global context. Passing this exam will demonstrate your ability to handle regulatory affairs challenges in a variety of geographical regions and countries. In this article, we will discuss how to pass the RAC-GS exam and provide exam details, exam objectives, who should take the exam, prerequisites and qualifications, and related books.
Exam Objectives:
- Understanding the global regulatory environment and compliance requirements
- Demonstrating knowledge of regulatory submission and approval processes
- Understanding the principles of regulatory affairs management
- Demonstrating knowledge of global product development and life cycle management
- Understanding the regulatory requirements for post-approval activities
The RAC-GS exam is suitable for regulatory affairs professionals who are responsible for managing regulatory affairs operations in a global context. The exam is designed to assess your understanding of regulatory requirements and principles in a variety of geographic regions and countries. The RAC-GS exam is not limited to any specific industry or product type, so anyone working in regulatory affairs can take the exam.
Before taking the RAC-GS exam, you must meet certain prerequisites and qualifications. To be eligible for the exam, you must have a minimum of three years of regulatory affairs experience in a global context. Alternatively, you can have two years of regulatory affairs experience and a master's degree or higher in a related field. You must also be a member of the Regulatory Affairs Professionals Society (RAPS).
Related Books:
- RAPS RAC Study Materials
- RAPS Online University
- The Regulatory Craft: Controlling Risks, Solving Problems, and Managing Compliance by Malcolm K. Sparrow
- Global Regulatory Issues for the Cosmetics Industry by C. Michel and M. Sadowski
- Pharmaceutical Regulations for the Emerging Markets by Michael Anisfeld and Victoria Vu
- Regulatory Affairs for Biomaterials and Medical Devices by Stephen F. Amato and Richard A. McFarland
Exam Details:
- Delivery Method: Computer-Based Testing (CBT)
- Exam Format: Multiple Choice Questions (MCQs)
- Exam Time: 3.5 hours
- Exam Cost: RAPS Member - $1,199; Non-member - $1,399
- Passing Mark: 70%
- Exam Location: Available at Pearson VUE test centers worldwide
To pass the RAC-GS exam, you must prepare well and study the exam objectives thoroughly. You can use the related books mentioned above as study materials. RAPS also provides study materials and online courses to help you prepare for the exam. On the exam day, you should arrive at the test center early and bring a government-issued photo ID. The exam consists of 150 multiple-choice questions, and you will have 3.5 hours to complete it. You
must answer at least 70% of the questions correctly to pass the exam. After the exam, you will receive your score immediately, and if you pass, you will receive a certificate from RAPS, which will recognize your knowledge and expertise in regulatory affairs on a global scale.
In conclusion, passing the RAC-GS exam can help you boost your regulatory affairs career and demonstrate your knowledge and expertise in a global context. By following the exam objectives, using study materials such as related books, and preparing well, you can increase your chances of passing the exam. If you meet the prerequisites and qualifications and are a member of RAPS, you are eligible to take the exam. The RAC-GS exam is delivered through computer-based testing and consists of 150 multiple-choice questions that you must complete in 3.5 hours. By passing the exam, you will receive a certificate from RAPS that recognizes your regulatory affairs knowledge and expertise on a global scale.