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Improving Performance, Reducing Risk
LRQA is a world leading, independent provider of professional assurance services including management system certification, validation, verification and training to bespoke and international standards and schemes.
Leading and Managing Risk through ISO 9001:2015 Quality Management System standard
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Learn about what constitutes to a cyber supply chain and the exploits taken by cyber-attackers to cause disruptions to your supply chain.
Iveco Trucks Australia is the first commercial vehicle manufacturer and distributor in Australia to successfully transition to ISO 9001:2015, certified by LRQA
Van Leeuwen became the first organisation in continental Europe to achieve certification against the revised ISO 9001:2015 standard.
Find out more about the new ISO 9001:2015 standard revisions and compare its differences with ISO 9001:2008.
Find out more about the new ISO 14001:2015 standard revisions and compare its differences with ISO 14001:2004.
Read about CPF's success from recognizing the importance to operate in a socially and environmentally responsible and sustainable manner.
Mitr Phol group has achieved success in multiple international standards with LRQA including ISO 9001, ISO 14001, ISO 22000, OHSAS 18001 and ISO 50001.
Keep up to date with latest industry news, insight and information from LRQA
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The International Aerospace Quality Group (IAQG) has now published AS9110:2016 and AS9120:2016. This completes the revision of the core Aerospace Standards and represents the revised quality standard for aviation, defence and space organisations.
Following a week of meetings in June 2016, during which ISO 45001 - the new occupational health and safety standard being developed by the International Organization for Standardization (ISO) - moved to a second draft international standard (DIS2) stage, ISO/PC 283/WG1, the Working Group responsible for developing the new standard, met three weeks ago in Lithuania.
The medical regulatory landscape is said to be undergoing its most significant overhaul in years. The new European Union (EU) Medical Device Regulation (MDR) and In Vitro Diagnostic Device Regulation (IVDR) have been four years in the making, and are likely to be published in Q1 2017.
This course will help you discover the significant new and enhanced requirements defined in IATF 16949:2016 compared with ISO/TS 16949:2009
Learn about the importance of process management and how you can improve process performance to support business objectives.
Learn about the fundamentals and benefits of structured approaches to problem solving in order to effectively use corrective and preventive processes to drive improvement within your organisation.
Discover how you can implement the Failure Mode and Effects Analysis (FMEA) methodology in your organisation.