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Baraa Nofal

Baraa Nofal

Regdesk Author

LinkedIn: https://www.linkedin.com/in/baraa-nofal-250789a3/

Baraa is a licensed pharmacist and a Regulatory and Quality Lead with over seven years of experience across the pharmaceutical, veterinary, and medical device sectors. PMP and PMI-PBA certified, she specializes in leading and coordinating global teams to deliver high-quality regulatory intelligence, proactive monitoring, and surveillance activities for medical devices, with a strong focus on the Middle East and Africa.  Baraa is driven by a commitment to excellence, continuously overcoming regulatory challenges and elevating standards within the Regulatory Affairs and Quality Assurance function.

Articles by this author

medical-device-regulations-in-cis-countries-2026-guide

Medical Device Regulations in CIS Countries 2026: Competent Authorities, Registration Pathways, and Market Entry Strategies

February 10, 2026

Read Medical Device Regulations in CIS Countries 2026: Competent Authorities, Registration Pathways, and Market Entry Strategies

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understanding-the-fda-asca-program-accredited-testing-reduced-risk-and-stronger-submission-confidence

Understanding the FDA ASCA Program: Accredited Testing, Reduced Risk, and Stronger Submission Confidence

February 4, 2026

Read Understanding the FDA ASCA Program: Accredited Testing, Reduced Risk, and Stronger Submission Confidence

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Important Things to Know Before Registering your Medical Device in Czech Republic

February 28, 2019

Read Important Things to Know Before Registering your Medical Device in Czech Republic

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Things You Should Know Before Registering Your Medical Devices in Spain

January 19, 2019

Read Things You Should Know Before Registering Your Medical Devices in Spain

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