< Back to all authors

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

where-mena-device-registrations-go-off-track-and-how to-stay-ahead 1

Where MENA Device Registrations Go Off Track And How to Stay Ahead

March 30, 2026

Read Where MENA Device Registrations Go Off Track And How to Stay Ahead

link
premarket-approval-what-manufacturers-need-to-know

Premarket Approval: What Manufacturers Need to Know

March 5, 2026

Read Premarket Approval: What Manufacturers Need to Know

link
changes-to-registration-requirements-in-northern-ireland

Changes to Registration Requirements in Northern Ireland

March 4, 2026

Read Changes to Registration Requirements in Northern Ireland

link
eda-updates-facilitation-mechanism

Egyptian Drug Authority Simplifies Certain Medical Device Registration Procedures

February 25, 2026

Read Egyptian Drug Authority Simplifies Certain Medical Device Registration Procedures

link
understanding-predicate-devices-in-510k-submissions

Understanding Predicate Devices in 510(k) Submissions

February 23, 2026

Read Understanding Predicate Devices in 510(k) Submissions

link
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

link
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

link

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

link

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

link
# #