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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.
Consumer electronics such as batteries, lighting, IT/AV, wiring and household appliances need to comply with regulatory and compliance requirements of India which are BIS – CRS (compulsory registration scheme) and BIS-ISI marking scheme before ...
SMETA – SEDEX Members Ethical Trade Audit is a methodology developed by SEDEX - Supplier Ethical Data Exchange as a centrally agreed audit protocol that can be shared amongst the SEDEX members. URS, under the group, is Affiliate Audit Company ...
‘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”