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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.
Automotive is a growing sector in India and around the world. With new technology and encouragement to produce the best, manufacturers need to validate and verify their components as a part of their R&D procedure. This includes testing of these...
BRSR Core is a mandatory sustainability reporting framework introduced by SEBI for India’s top listed companies. It focuses on key ESG metrics such as energy use, emissions, workforce well-being, supply chain responsibility, and ethical governa...
‘CE’ marking is a mandatory mark for many designated products placed in European Economic Area (EEA) which ensures the product is thoroughly assessed for Essential Health & Safety Requirements (EHSR) according to the EU Regulations.
“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”