Overview

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Extension of the transition periods for the Medical Device Regulation (MDR)
Good news for medical device industry: The European Commission has approved a proposal that will ...
Feb 23, 2023
How to access the Japanese market with medical devices (for overseas companies)
In Japan, the Ministry of Health, Labor and Welfare(MHLW) regulates the manufacture, sale, and ...
Feb 23, 2023
# MDSAP- Medical Device Single Audit Program
# ISO 13485
DQS at the MEDTECH MEETUP 2023 in Brussels
The MedTech Meetup in Belgium is a unique event for the medical device, IVD medical device and ...
Feb 16, 2023
Remote audit - Prerequisites, opportunities and limitations
Remote audits have become an integral part of digitization and agile working.  What is meant is ...
Feb 14, 2023
# Environmental management
"Cyber Security Standard Development" DQS at the GHWP Annual Meeting in Riyadh
The Global Harmonization Working Party (GHWP) is a not-for-profit organisation with the mission to ...
Feb 10, 2023
Occupational health & safety and compliance: closing the gaps
Compliance with legal obligations by top management or the employer is an absolute prerequisite for ...
Jan 26, 2023
# Occupational Health & Safety
# Occupational health and safety in the integrated management system

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