Pharmaceutical Regulatory Affairs Certification
Program Overview
This program provides with knowledge and insight into the current U.S. Professional Regulatory Affair pathways for prescription and over-the-counter drugs, biologics, medical devices, as well as combination products. At the end of this program, students will have a good understanding of the regulatory framework around drug development, regulatory submissions, CTD, IND, NDA & ANDA, FDA regulatory submission requirements, Chemistry and Manufacturing Control and Post approval compliance and regulatory requirementds, current Good Manufacturing Practices (cGMP) and quality concepts.
Anytime. Anywhere
Self-Paced
Course Length
36 Weeks
Direct Access to Instructors
Online Support
Career Service
Networking
Anytime. Anywhere
Self-Paced
36 Weeks
Course Length
Online Support
Direct Access to Instructors
Career Service
Networking
Why Choose Our RA Program?
1. Flexibility to Fit Your Life
Our online learning environment gives students the option to learn completely at their own pace, anywhere and at any time of the day. Learners will have access to our subject matter experts who are there to provide support and answer any subject related questions.
2. Learn from Expert Faculty
Our program is led by experienced Regulatory Affairs experts, with decades of experience, who bring their real-world knowledge into the classroom. They’ll guide you every step of the way, ensuring you graduate with the skills, compassion, and confidence needed to succeed.
3. Career Services and Networking
We developed strong partnerships with industry-leading companies in pharmaceutical and clinical field. We work directly with these organizations to provide opportunities to our graduates.
Curious to Learn More?
Your Path to a Rewarding Career
Regulatory Affairs professionals are the backbone of compliance and innovation, ensuring that pharmaceutical, biopharmaceutical, and medical device products meet all FDA and global regulatory requirements. With a growing demand across the country, your expertise in Regulatory Affairs will be invaluable in a variety of roles:
Job Opportunities
- Regulatory Affairs Scientist
- Regulatory Affairs Associate
- Regulatory Affairs Specialist
- Regulatory Affairs Project Manager
- Regulatory Affairs Manager
- Regulatory Affairs Project Coordinator
- Regulatory Affairs Director
- Compliance Specialist
- Compliance Associate
What do regulatory affairs professionals earn?
Regulatory professionals’ average compensation continues to increase, according to RAPS’ recent compensation survey. The average total compensation for US-based regulatory professionals in recent years ranged from $292,625 for vice presidents to $108,627 for specialists. Respondents reported an average base salary increase of 5.6% from year to year.
Networking
- We developed strong partnerships with industry-leading companies in pharmaceutical and clinical field. We work directly with these organizations to provide opportunities to our graduates.
What Sets Us Apart?
- Flexible and Modern Learning: Benefit from an online model that fits your lifestyle.
- Expert Instructors: Learn from industry professionals with years of practical experience in the field.
- Career Services: Access resume support, mock interviews, job search guidance, and exclusive employer connections.
- Industry-Relevant Curriculum: Stay ahead with content designed to meet current FDA and global regulatory standards.
- Networking Opportunities: Connect with peers, alumni, and professionals through virtual events and mentorship programs.
Join a program designed to empower you with the skills, knowledge, and experience to transform your career.
Complete the form to learn more about enrollment, financial aid, program details, and more.
