BVQA Vietnam was licensed to issue Product Certification of Construction materials
BVQA Vietnam was licensed to issue ISO 45001 certification (Occupational Health and Safety Management Systems)
BVQA is ready for issuing ISO 22000:2018 & HACCP certificates with accrediation of BoA and recognization of IAF.
With over two hundred diseases spread through the food chain, it’s clear that safe, sustainable food production is one of our greatest challenges. Globalization of the food trade further complicates food safety and the new edition of ISO 22000 on food safety management systems presents a timely response.
As the three-year transition for ISO 9001 and ISO 14001 moves into its final year, IAF (the global association for developing the principles and practices for the conduct of conformity assessment) has passed a resolution that as of 15 March 2018, BVQA must conduct all ISO 9001 and ISO 14001 initial, surveillance and recertification audits to the new versions - ISO 9001:2015 and ISO 14001:2015.
BVQA is ready for issuing ISO 14001:2015 certificates with accrediation of BoA and recognization of IAF
BVQA is ready for issuing ISO 9001:2015 certificates with accreditation of BoA and recognition of IAF
The latest edition of ISO 9001, ISO's flagship quality management systems standard, has just been published. This concludes over three years of revision work by experts from nearly 95 participating and observing countries to bring the standard up to date with modern needs.
ISO 14001:2015 which sets out the requirements for an environmental management standard, is one of the world’s most widely used standards and a key business tool for many organizations. With more than 300000 certificates currently issued around the world, it ranks high on the agenda of many organizations worldwide who place importance on their environmental impact.
LED Products, an environmentally friendly choice towards Energy management systems ISO 50001 Please visit:
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EN ISO 13485:2012 will soon be the harmonized standard for quality management systems under EC Directives 90/385/EEC (Active Implantable Medical devices), 93/42/EEC ( Medical Devices) and 98/79/EC (In Vitro Diagnostic Medical Devices). However as it contains no new requirements manufacturers that have been successfully audited by a Notified Body will not normally require any changes to their quality management system.