Frequently Asked Questions
What are the qualifications required to apply for the RA certificate?
- Graduated students with Bachelor degree, Masters, or PHD including any life science such as Pharmacy, Biotechnology, Biology, Chemistry, or any equivalent majors.
- An earned degree with a GPA of at least 3.25 from an accredited institution.
What are the Regulatory Affairs Program Provided by RADEX Institute?
- Regulatory Affairs of Drugs and Medical Devices - USA & Europe (14 Credit).
- Regulatory Affairs of Drugs and Medical Devices - MENA Region (5 Credit).
What is the duration of the RA certificate program?
Regulatory Affairs of Drugs and Medical Devices - USA & Europe:
Three hours lecture with three more hours workshop once a week.
The duration is 9 months (36 Weeks):
- 8 months theoretical.
- 1-month practical take-home RA project.
Regulatory Affairs of Drugs and Medical Devices - MENA Region:
Three hours lecture with two more hours workshop once a week.
The duration is 4 months (14 Weeks):
- 3 months theoretical.
- 1-month practical take-home RA project.
Do I have to register in the 2 Programs?
You can choose to register in "Regulatory Affairs of Drugs and Medical Devices - USA & Europe" program ONLY.
Or
You can register in "USA & Europe" program and then enroll in "MENA Region" program, as MENA Region Program is optional.
* (Regulatory Affairs - MENA Region Program is Optional): Students who choose to enroll in "MENA Region" Program in May, must first complete "USA & Europe" Program.
Can I take "MENA Region" program without Registering in "USA & Europe" program?
Students who choose to enroll in "MENA Region" Program in May, must first complete "USA & Europe" Program.
What is the duration of the RA certificate program?
Regulatory Affairs of Drugs and Medical Devices - USA & Europe:
Three hours lecture with three more hours workshop once a week.
The duration is 9 months (36 Weeks):
- 8 months theoretical.
- 1-month practical take-home RA project.
Regulatory Affairs of Drugs and Medical Devices - MENA Region:
Three hours lecture with two more hours workshop once a week.
The duration is 4 months (14 Weeks):
- 3 months theoretical.
- 1-month practical take-home RA project.
How will the Regulatory Affairs Training Certificate benefit my career advancement?
The professional certification we offer helps demonstrate your commitment to job performance, increase the quality of your work, to be recognized as the exceptional RA specialist.
This course may be helpful for both those seeking a new career or transitioning to the RA positions within their organization.
What are the methods of training available?
- Live interactive online sessions.
What are the fees for the "Enrollment Agreement" Application?
The application fees are a non-refundable 100$. However, we have waived the application fees until August 1st, 2022.
What are the Tuition Fees for Graduate certificates?
Tuition fees for Regulatory Affairs of Drugs and Medical Devices - USA & Europe are $8,615.
- Ask more about our "Payment Plan", we offer a MONTHLY payment installment option.
Tuition fees for Regulatory Affairs of Drugs and Medical Devices - USA & Europe are $3,162.
- Ask more about our "Payment Plan", we offer a MONTHLY payment installment option.
Do I have to pay in full or do you have installments and payment plan?
Ask more about our "Payment Plan", we offer a MONTHLY payment installment option.
Was your question not answered?
Please reach out to us with any remaining concerns or additional questions. Feel free to contact us at Admission@radexinstitute.com
Copyright © 2022 RADEX Institute - All Rights Reserved.
This website uses cookies.
We use cookies to analyze website traffic and optimize your website experience. By accepting our use of cookies, your data will be aggregated with all other user data.