Frequently Asked Questions

1. Regulatory Affairs of Drugs and Medical Devices (USA, Europe, & GCC) Professional Training Program.
2. Pharmacovigilance and Vigilance, an International Perspective (Europe, KSA, UAE, & Jordan) Professional Training Program.
3. Customized Training aligning with pharmaceutical companies’ needs.

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Graduated students with bachelor’s degree, master’s degree, or PHD including any life science such as Pharmacy, Biotechnology, Biology, Chemistry, or any equivalent majors.

Live interactive online sessions.

The RADEX Regulatory Affairs Professional Training Course covers a wide range of fields, including drugs, biologics, medical devices, vitamins, natural products, dietary supplements, cosmetics, advertising, Good Manufacturing Practices (GMP), and clinical trials.

• Stability and Confidence: Since the regulatory affairs topics covered by RADEX professional training programs are worldwide in scope, graduates who choose to switch workplaces or countries won’t have to start from scratch because they’ll already possess all the necessary full knowledge.
• More Career Opportunities and become “In-demand”: RADEX Professional Training Programs empower scholars, scientists, and professionals by experiencing all Regulatory Affairs types and Pharmacovigilance Jurisdictions that will help our graduates stay competitive and open a wide horizon of job opportunities to choose from that aspires them to be global leaders who can tackle complex challenges.

RADEX Regulatory Affairs Professional Training Program provides a comprehensive insight into regulations set forth by prominent authorities such as the US Food and Drug Administration (USFDA), European Medicines Agency (EMA), Saudi Food and Drug Authority (SFDA), and UAE’s Ministry of Health and Prevention (MOHAP).

Likewise, the RADEX Pharmacovigilance and Vigilance Professional Training Program delves into regulations from the European Medicines Agency (EMA), Saudi Food and Drug Authority (SFDA), UAE’s Ministry of Health and Prevention (MOHAP), and Jordan Food and Drug Administration (JFDA).

Considering our MENA region location, where regulations are predominantly influenced by USFDA and EMA guidelines, integrating these standards into our RADEX program is both imperative and strategically sound. Given that these authorities are globally recognized as leaders in regulation, adhering to their standards will substantially boost your chances of securing employment opportunities.

1. Regulatory Affairs of Drugs and Medical Devices (USA, Europe, & GCC) Professional Training Program – 26 weeks.
2. Pharmacovigilance and Vigilance, an International Perspective (Europe, KSA, UAE, & Jordan) Professional Training Program – 4 weeks.
3. Customized Training – The duration for these programs is determined based on the client’s requested topics and the chosen timeframe, whether for online or onsite delivery.

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1. Regulatory Affairs of Drugs and Medical Devices (USA, Europe, & GCC) Professional Training Program.

• Times: 2 days/ Week.
• Duration: 3 hours / day. 6-9 pm (Riyadh Time)

2. Pharmacovigilance and Vigilance, an International Perspective (Europe, KSA, UAE, & Jordan) Professional Training Program.

• Times: 2 days/ Week.
• Duration: 4 hours/ day. 6-10 pm (Riyadh Time)

Asma Abu-Staiteh, MSc. In Regulatory Affairs (Northeastern University, USA).

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RADEX Professional Training Programs Certificates accreditation is from Philadelphia University in Jordan and are endorsed by the Jordanian Ministry of Higher Education. Furthermore, our certificates undergo legalization procedures with the Ministry of Higher Education and the Ministry of Foreign Affairs to affirm the recognition of our certificates globally worldwide.

RADEX programs offer practical training through workshops and critical thinking projects, guiding students on navigating online portals for each regulatory authority. Additionally, assignments are provided to complete registration application forms. Each student receives an annex containing a comprehensive Common Technical Document (CTD) file or Pharmacovigilance System master File for educational purposes, empowering them to apply their knowledge effectively in the field of Regulatory Affairs and Pharmacovigilance, respectively.

RADEX has a diverse group of graduates hailing from more than 17 countries, including fresh graduates, specialists, and managers. The certificate obtained from our program is internationally recognized, enabling graduates to pursue opportunities across the globe. As most countries align their regulations with those of USFDA and EMA, which are extensively covered in our course, our graduates are well-equipped to navigate regulatory affairs in various regions.

The professional certification we offer helps demonstrate your commitment to job performance, increase the quality of your work, and to be recognized as the exceptional Regulatory Affairs specialist.

These courses may be helpful for both those seeking a new career or transitioning to Regulatory Affairs positions within their organization.

Also, if you are looking to secure a promotion, RADEX Professional Training Programs can help you gain the knowledge and skills required to move up the ladder at your current company. Most companies prefer a postgraduate certificate to grant a promotion to management positions.

1. Regulatory Affairs of Drugs and Medical Devices (USA, Europe, & GCC) Professional Training Program.

9,000 SAR/ AED – 1700 JOD – 2,400 $

2. Pharmacovigilance and Vigilance, an International Perspective (Europe, KSA, UAE, & Jordan) Professional Training Program.

4,000 SAR/ AED – 750 JOD – 1,060 $

3. Customized Training

The fees for these programs are determined based on the client’s requested topics and the chosen timeframe, whether for online or onsite delivery.

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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 info@radexregaffairs.com

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