Intertek Blog
The Intertek Blog is a trusted source for insights on product safety, quality, sustainability, innovation, and compliance. The articles written by our experts explore industry trends, emerging technologies, regulatory developments, and best practices, delivering the knowledge and perspective you need to stay informed and inspired.
Most Recent Posts
06 Nov 2025
Building Artificial Intelligence Features and Functionality into Medical Devices – Part 1
The Necessity of Embedded Design and Cyber-Aware Risk Management
04 Nov 2025
Making Light Work: Accelerating Reliability with HALT and FMVT
Why Accelerated Stress Testing Matters
31 Oct 2025
Unlocking the Brazilian Market: Inmetro Certification for Medical Devices in 2025
Brazil's Growing Demand for Medical Devices
30 Oct 2025
Connecticut Enacts New Rules on Battery-Powered Smoke Detectors/Alarms
What Manufacturers, Distributors, and Facility Owners Need to Know
28 Oct 2025
Medtech at 50: How Innovation, AI, and Patient-Centered Care Are Redefining the Future of Health
A Milestone Moment for Medtech as Innovators, Regulators, and Patient Advocates Converge to Chart a Bold, Human-centered Future
27 Oct 2025
Biotechnology in cosmetics: Hyaluronic Acid Ingredients
Enabling Quality for Biotech Beauty Products – Part 2
23 Oct 2025
Changes to Robots – How the New Framework Addresses Autonomous Systems – Part 4
Responsible Robotics – Who Owns the Risk When Machines Change?
22 Oct 2025
A Smarter Path to Hurricane-Region Building Product Approvals
A structured three-step process helps manufacturers streamline approvals, reduce costs, and shorten timelines
21 Oct 2025
Understanding the 2023 Updates to the CSA C22.2 No. 301 Standard – Part 6
The Integration of Robotics in Industrial Environments
16 Oct 2025
Changes to Robots – How the New Framework Addresses Autonomous Systems – Part 3
Cyber Meets Safety – Securing Intelligent Systems by Design
14 Oct 2025
Inside the Panel: Technical Considerations for Certifying Custom Switchboards
Meeting the safety requirements of UL 891 and CSA C22.2 No. 244
09 Oct 2025
Key Insights and Best Practices for Prop 65 Compliance of Medical Devices
A Practical Guide to Staying Ahead of California’s Prop 65 Requirements
02 Oct 2025
Understanding the New Conformity Assessment Modules under the EU Machinery Regulation
Enhancing transparency and harmonising conformity pathways with other EU product legislation
30 Sep 2025
Industry 5.0: When to Start Your EU Compliance Journey
How forward-thinking manufacturers can leverage these regulations as catalysts for innovation