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Binding obligations in ISO 14001 - What does the standard require?
Compliance obligations to interested parties is one of the core topics in ISO 14001, requiring the o
Mar 29, 2023
# Environmental management
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 giv
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 distr
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 digit
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 the
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

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