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EU MDR Certification Process Explained: CE Marking Requirements for Medical Devices

The European Medical Device Regulation (MDR) (EU) 2017/745 represents a significant transformation o
Apr 02, 2026
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AWS and Azure Are ISO 27001 Certified — But That Doesn't Mean Your Company Is

"We run everything on AWS. AWS has ISO 27001 certification. So we should be covered, right?"This is
Mar 23, 2026
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2026 EU MDR Simplification Proposal: 5 Key Impacts on Medical Device Manufacturers

For medical device manufacturers in Hong Kong and the Asia-Pacific region planning to export or curr
Mar 20, 2026
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NIS-2 for Managing Directors: Duties, Liability, and Implementation

With the entry into force of the NIS2 Implementation Act (NIS2UmsuCG) on December 6, 2025, cybersecu
Mar 16, 2026
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How Multi-Site Sampling Works in ISO Audits and What It Means for Your Business

If your organisation operates across multiple office locations, one of the first questions you’ll
Mar 13, 2026
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AI Act and AI-Enabled Medical Devices - Current Regulatory Status

Regulation (EU) 2024/1689 (the AI Act), which entered into force on 1 August 2024 as the world's fir
Mar 12, 2026
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