Frequently Asked Questions

  • 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.
  • Regulatory Affairs of Drugs and Medical Devices – USA & Europe (14 Credit).
  • Regulatory Affairs of Drugs and Medical Devices – MENA Region (5 Credit).

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.

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.

“USA & Europe” Program is a pre-requisite for the optional Regulatory Affairs – MENA Region Program. So, Students who choose to enroll in “MENA Region” Program in May, must first complete “USA & Europe” Program.

Students who choose to enroll in “MENA Region” Program in May, must first complete “USA & Europe” Program. 

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.

  • Live interactive online sessions.
The application fees are a non-refundable 100$.

Tuition fees for Regulatory Affairs of Drugs and Medical Devices – USA & Europe are $5,879.

* 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.

Ask more about our “Payment Plan”, we offer a MONTHLY payment installment option.

Please reach out to us with any remaining concerns or additional questions. Feel free to contact us at [email protected]

Founded in the year 2018, RADEX Institute has provided training, consultation, and registration services
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