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Regulation (EU) 2023/607 - Extension of the transitional period MDR (EU) 2017/745
With the publication of Regulation (EU) 2023/607 in the Official Journal of the European Union, a lo
Apr 17, 2023
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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
umwelt-header-blog-dqs-mit gruenen pflanzen bepflanzte treppe bestehend aus weissen steinen
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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 giv
Feb 23, 2023
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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 dist
Feb 23, 2023
# MDSAP- Medical Device Single Audit Program
# ISO 13485
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Remote audit - Prerequisites, opportunities and limitations
Remote audits have become an integral part of digitization and agile working. What is meant is the d
Feb 14, 2023
# Environmental management
remote audit -dqs-digital networking worldwide
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Core Technology Molding Corp Wins 2022 North Carolina Business Award
As the business climate changed over the last few years, companies have had to adapt and make the ne
Feb 13, 2023
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Core Technology Molding Corp's Merck Assemblies
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