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Medical Devices Quality Management System ISO 13485 is an effective management tool to address risk throughout the production process and ensures compliance to regulatory, safety and medical product related requirements. ISO 13485 Certification by URS is well recognized worldwide and is accredited by international accreditation board i.e. UKAS.
The EU’s Carbon Border Adjustment Mechanism (CBAM) requires exporters to disclose the embedded carbon emissions of their products. Compliance is essential for businesses exporting to the EU to avoid financial penalties and maintain market acces...
EMI EMC requirement is to verify and control the side effects caused upon electronics and electrical equipment when they are either interconnected or come into close proximity. Similar to identify and control side effects caused into environmen...
After Brexit, the UKCA Mark (United Kingdom Conformity Assessment) is a new product marking scheme announced by the United Kingdom which is applicable to all goods/ products shipped in Great Britain (England, Wales and Scotland). At present, t...
“Be advised that as per the new requirement of IAF/ISO Joint Communique Dated 22nd February 2024, In consideratio...
URS Certification Ltd gets NABCB accreditation for ISO 21001 Standard.
We are deeply shocked by the tragic plane crash that occurred in Ahmedabad. Our hearts go out to the Passengers, ...
“Be advised that as per the new requirement of IAF/ISO Joint Communique Dated 22nd February 2024,In consideration of requirement of clause 4.1 and 4.2 Understanding the context of organisation and needs and expectation of interested parties, it is important for you to determine whether climate change is a relevant issue and consider where interested parties can have requirements related to climate change”