Healthcare
Safety and quality are non-negotiable in the medical devices industry.
Regulatory requirements for medical devices are increasingly stringent throughout every step of a product’s life cycle, including service and delivery.
The International Organization for Standardization (ISO) is an independent organization dedicated to publishing quality and risk management standards for product development in a variety of industries, including medical devices.
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Standards Library
Access the latest European Voluntary Standards. All documents are officially verified and regularly updated to reflect current regulations.
18
Standards
5
Categories
PDF
+ DOCX
Type
Name
Language
Format
NEW ISO, Aerospace, Healthcare
ISO 9001 2026 versus ISO 9001 2015
Quality management systems – Requirements
English
$80.00
including VAT
$45.00
including VAT
$120.00
including VAT
Aerospace
EN 3475-408:2025 versus EN 3475-408:2005
Aerospace series — Cables, electrical, aircraft use — Test methods Fire resistance
English