Vulnerability Disclosure: Overview of Main Requirements
In today’s digitally connected healthcare landscape, the integration of medical devices with networked systems and electronic health records has revolutionized…
Process Validation Series: Installation Qualification
In regulated industries like medical device manufacturing, ensuring product quality and compliance with stringent regulatory standards is paramount; within the…
ROHS Compliance: An essential Guideline for Medical Device Manufacturers
RoHS compliance has become a focal point for companies worldwide, shaping their production methods and product design to align with…
ISO 27001 Scope Template: A Practical GuidelineĀ
One of the most important document related to ISO 27001 is related to the definition of the scope of an…
ISO 14971 : Risk Management for Medical Devices
The approval of ISO 14971 for medical device risk management in December 2019 marked a significant milestone in ensuring the…
ISO 27001 Vulnerability Assessment
In the intricate realm of information security, where digital landscapes evolve and cyber threats loom large, the ISO 27001 standard…
Asset Management according to ISO 27001:2022
In the complex landscape of information security, where data reigns supreme, the ISO 27001 standard stands as a beacon guiding…
Cybersecurity Threat Model Implementation: FDA Requirements
The Food and Drug Administration (FDA) plays a pivotal role in safeguarding public health through the regulation of medical devices,…
Business Continuity Plan: Strategies for Implementation
As the digital era continues to expand, information security stands as a cornerstone of modern business strategy and having a…
Medical Device Lifetime: An Overview
The Integral Role of Lifetime in Medical Device Utilization The lifetime of a medical device is a critical period during…
