Our Blogs

December 23, 2025
Exploring the Regulatory Framework for Medical Software: Challenges and Solutions

A well-prepared Performance Evaluation Report (PER) is essential for demonstrating the safety, effectiveness, and regulatory compliance of IVD medical devices in the Saudi market.

December 23, 2025
Exploring the Regulatory Framework for Medical Software: Challenges and Solutions

A well-prepared Performance Evaluation Report (PER) is essential for demonstrating the safety, effectiveness, and regulatory compliance of IVD medical devices in the Saudi market.

July 6, 2025
Top 6 ISO 13485 Requirements Every Medical Company Must Follow

Discover the six most critical ISO 13485 requirements that medical device companies must implement to ensure regulatory compliance, product quality, and patient safety. This guide simplifies the standard’s key elements for smooth certification and market readiness.

April 16, 2025
Key Elements of Performance Evaluation Reports

A well-prepared Performance Evaluation Report (PER) is essential for demonstrating the safety, effectiveness, and regulatory compliance of IVD medical devices in the Saudi market.

January 28, 2025
Understanding SFDA Requirements for Distributors of Medical Devices in Saudi Arabia

Saudi Arabian distributors play a crucial role in the healthcare supply chain, ensuring that medical devices reach the market in compliance with local regulations.

December 24, 2024
Saudi Arabian Licensing Requirements for Medical Device Establishment License

Saudi Food and Drug Authority ensures that medical devices used in the Kingdom of Saudi Arabia meet high standards of safety and quality in today's evolving healthcare landscape

December 3, 2024
Understanding Medical Device Marketing Authorization (MDMA) in Saudi Arabia

Medical Device Marketing Authorization (MDMA) ensures that medical devices entering the Saudi market meet regulatory standards set by the Saudi Food and Drug Authority (SFDA).

November 4, 2024
Understanding the Role of the Authorized Representative (AR) in Medical Device Registration

Authorized Representatives (ARs) play an important role in the regulatory process. Medical device industry professionals or those looking to launch products in new markets

October 21, 2024
SFDA's Post-Market Clinical Follow-up (PMCF): Ensuring Medical Device Safety and Effectiveness

Post-Market Clinical Follow-up (PMCF) is a crucial aspect of maintaining the safety and effectiveness of medical devices after they have been introduced into the market.

October 13, 2024
Saudi Arabia's Unique Device Identification (UDI) Role in Medical Device Safety

SFDA has introduced stringent regulations for Saudi-DI for all medical devices marketed within the Kingdom.

September 25, 2024
Understanding Self-Test Devices: A Growing Trend in Healthcare

Self-testing devices, also known as home diagnostic devices, allow individuals to perform health tests on themselves, interpret the results, and take action based on the results.

September 17, 2024
Role of Audit Reports and SOPs in a Quality Management System

Standard Operating Procedures (SOPs) and audit reports are two of these critical components. By working together, they ensure compliance with best practices, compliance with regulatory requirements, and continuous improvement within the organization.

August 4, 2024
Comparing SFDA’s IVD Regulatory Framework with IVDR (European Standards)

Reliable diagnostics are essential for public health, making it imperative to understand the regulatory frameworks that govern these devices.

August 1, 2024
Understanding ISO 13485: Ensuring Quality and Safety in Medical Devices

An ISO 13485 quality management system (QMS) specifies requirements for the design and manufacture of medical devices

August 1, 2024
Understanding Accuracy and Precision in IVD Devices: Implications for Safety

Modern healthcare relies heavily on in vitro diagnostic (IVD) devices to provide essential data that allows clinical decisions to be made.

July 28, 2024
Inside NCMDR: Everything You Should Know About Medical Device Reporting

Essentials of the National Medical Device Reporting (NCMDR) system, explaining its purpose and key requirements for reporting medical devices.

July 28, 2024
Classification and Registration of Medical Devices: Decoding the SFDA's Process

This outlines the Saudi FDA's classification and registration process for medical devices, offering key insights for manufacturers navigating the regulatory landscape.

Bio-Standards Blog

Here you’ll find the latest blogs about compliance news and guidance for all medical industries.

December 23, 2025
Medical Device
Exploring the Regulatory Framework for Medical Software: Challenges and Solutions

A well-prepared Performance Evaluation Report (PER) is essential for demonstrating the safety, effectiveness, and regulatory compliance of IVD medical devices in the Saudi market.

Latest blog posts

November 4, 2024
Understanding the Role of the Authorized Representative (AR) in Medical Device Registration
Medical Device
October 21, 2024
SFDA's Post-Market Clinical Follow-up (PMCF): Ensuring Medical Device Safety and Effectiveness
Medical Device
October 13, 2024
Saudi Arabia's Unique Device Identification (UDI) Role in Medical Device Safety
Medical Device
September 25, 2024
Understanding Self-Test Devices: A Growing Trend in Healthcare
Medical Device
September 17, 2024
Role of Audit Reports and SOPs in a Quality Management System
Medical Device
August 4, 2024
Comparing SFDA’s IVD Regulatory Framework with IVDR (European Standards)
Medical Device