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Professional Regulatory Affairs
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COURSES
Medical Device Regulation Masterclass – MENA
Master the Regulatory Landscape for Medical Devices in the MENA Region
Overview
This masterclass is designed to provide individuals with a solid and comprehensive framework in medical device regulatory affairs The course will address market information, technical documentation, and guidelines from relevant authorities in the MENA region, equipping you with the essential knowledge to navigate the regulatory landscape effectively.
For Aspiring Professionals:
• Build a strong foundation in MENA-specific medical device regulations and market entry requirements.
• Learn how to navigate the medical device registration process and prepare technical documentation for timely approvals.
For Experienced Professionals:
• Gain valuable insights from expert-led case studies, focusing on regulatory challenges and solutions in the medical device industry.
• Enhance your compliance strategies by staying updated on the latest regulatory trends and best practices in the MENA region.
Key Benefits:
Expert Insights: Learn from seasoned professionals with real-world experience in MENA medical device regulations, providing you with practical knowledge to navigate the industry.
Regulatory Updates: Stay informed on the latest MENA and EU medical device regulations to ensure ongoing compliance and market readiness.
Registration & Importation Mastery: Gain expertise in the medical device registration and importation procedures for MENA countries, ensuring a smooth path to market access.
Dossier & Certification Knowledge: Understand technical dossier requirements, including CE marking and ISO certifications, to streamline the approval process.
Quality Standards & Compliance: Enhance your knowledge of regional quality standards and compliance strategies to accelerate market entry.
Career Advancement: Strengthen your regulatory affairs expertise, positioning yourself for career growth in the medical device industry.
Is this course for you :
This Course Is Ideal for You If:
- You are a medical or science graduate starting a career in regulatory affairs for medical devices.
- You are new to a regulatory affairs department or to the MENA region’s medical device regulations.
- You are a fresh graduate in pharma, biomedical engineering, or a related field, looking to enter the medical device industry.
- You are an operations, marketing, or business development professional in the medical device industry.
- You are involved in internal or external audits of medical devices and need regulatory insights.
Why Choose Us?
• Expert Guidance: Our course is led by experienced professionals with real-world regulatory expertise in the MENA region.
• Comprehensive Approach: We provide a holistic view of MENA and EU medical device regulations, ensuring you cover all key aspects.
• Career Advancement: Our masterclass equips you with the knowledge and skills to advance your career in regulatory affairs and ensure compliance with international standards.
Regular Price:: 9,310.00 AED
Start Date: June 14th 2025
End Date: July 6th 2025
Location: Online Course
Modules: 8 module (comprehensive topics)
Duration: One month
Time: Sat & Sun (10 AM - 2 PM) Dubai Time
🔥 Early Bird Price: 7,913.50 AED
Start Date:01 March 2025
End Date: 31 March 2025
Start Date:01 March 2025
End Date: 31 March 2025
Download Our Brochure
- You can easily download our brochure by clicking the button below. Alternatively, feel free to reach out to us via WhatsApp for assistance.
Obtain a Certificate Upon Completion
Upon successfully completing our course, you will receive a prestigious certificate that:
- Recognizes your achievements and newly acquired skills
- Serves as tangible proof of your expertise
- Prestigious certificate from Dubai Pharmacy College.
Enroll today to Professional Regulatory Affairs GCC Course Certification
Frequently asked questions
Everything you need to know about our top-rated Webflow Masterclass course.
This masterclass is ideal for professionals working in or aspiring to work in medical device regulatory affairs in the MENA region, including regulatory specialists, quality assurance professionals, and those involved in market access for medical devices.
A background in medical devices, regulatory affairs, or related fields would be beneficial. The course is designed to provide comprehensive knowledge, suitable for both newcomers and experienced professionals.
The course is delivered online, allowing for flexible participation.
The course covers medical device regulations in the MENA region, EU regulations overview, market insights, registration procedures, technical dossier requirements, importation procedures, and quality standards.
Yes, the course includes information on registration steps and procedures for medical devices in various MENA countries.
You’ll gain in-depth knowledge of PV processes, GCC-specific regulations, a recognized certification with CME points from Dubai Health Authority, practical experience through case studies, and increased employability in the pharmaceutical industry.
Yes, the course provides a comparative analysis of EU and MENA medical device regulations and their implications for market access and compliance.
Yes, the course covers technical dossier requirements and guidance on obtaining necessary certifications like CE and ISO.
Yes, the course provides an overview of importation procedures for medical devices as per the competent authorities in the MENA region.