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MedQtech Knowledge Hub for Compliance & Quality Management Information, News and Downloads

ISO13485:2016
Certified

Whether you are just starting on your regulatory compliance journey or looking for guidance on specific rules and compliance regulations or seeking advice on how to implement a compliant quality management system, these materials are designed to help you.

This knowledge hub includes a selection of blog posts, news articles and white papers from our consultancy team to help give you inspiration and support for your medical device compliance journey.

Blogs

Read the latest articles by our quality and regulatory specialists for their insights on compliance requirements in the medical device industry.

Medical Device eQMS

5 advantages of an effective eQMS for Medical Device Companies

ISO 13485 QMS

8 key considerations when implementing an ISO 13485 QMS

Medical Device Labelling

Medical Device Labelling – An Introduction to the Essentials

MDR Classification

How to classify a medical device according to MDR 2017/745

Our medical device customers are based right across the Nordics and beyond.

To get started we would recommend a consultative led open discussion about your medical device business goals.

Knowledge Hub