14 July 2019 | GQS SIngapore

WRAP, SMETA, SA 8000, BSCI Certification Singapore, Manila, Batam, Batangas, Yangon

Dec 09

In: BSCI , GRS Global Recycling Standards , SMETA 6.0 , WRAP
By: administrator
Date: 9 December 2019
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SMETA, WRAP, GRS, SA 8000, BSCI Certification Manila, Singapore, Myanmmar

GQS Singapore is one of the oldest consulting firm providing services in Social compliance certification such as SMETA 6.0 Sedex Members Ethical Trade Audits, WRAP Worldwide Responsible Accredited Production, SA 8000 Social Accountabilit...

Nov 29

In: ISO 22559
By: administrator
Date: 29 November 2019
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ISO-TS 22559-1:2004, ISO 8100 Safety requirements for Lifts, Escalator Certification

ISO/TS 22559-1:2004 Safety requirements for Lifts or Escalator Certification GQS Singapore becomes the first to kick start ISO 22559 Certification consultancy for Lifts and Escalators certification and consultancy We would support Lift and Escalator manufacturers or Installation companies to Identif...

Nov 29

What type of R2 SERI certifications, you should consider?

What type of R2 SERI certifications, you should consider? It has been seen in the past few years that the most common certification in the e-waste recycling world is Responsible Recycling along with the e-Stewards. Moreover, certifications such as 14001 and OHSAS 18000 are also the test that recycle...

Nov 25

In: ISO 13485
By: administrator
Date: 25 November 2019
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How ISO 13485 is different from ISO 9001 ?

ISO 13485 is a great quality management standard for the manufacturer of medical devices. The manufacturer of the medical devices must be able to provide evidence that the devices are consistently following the safety and quality standards performing as per the standard for the customers or patients...

Nov 25

In: ISO 13485
By: administrator
Date: 25 November 2019
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Who requires ISO 13485?

A great quality management system is a group of policies and methods which will help assist an organization to match the demands of stakeholders. In some countries of the European Union and Canada, it’s a legal obligation to have quality management in the case of the manufacturing of medical d...

Nov 25

In: ISO 13485
By: administrator
Date: 25 November 2019
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Why you should get certified to ISO 13485?

ISO 13485 is willingly chosen certification process for medical devices, where most of the quality management system requirements and display compliance to medical devices testaments. Apart from harmonizing regulatory requirements, there are various other great benefits such as meeting the expectati...

Nov 25

What are the Best Systems for ISO 13485 Compliance?

A business can greatly gain certification and compliance with ISO 13485 over various deductions. Organizations will have to strive hard to maintain the quality method on paper or an offer that has an inclusion of various schemes to keep employee training along with the quality management and documen...

Nov 25

ISO 13485:2016: What are the tips to optimize your medical device quality management system?

It’s one of the important questions that have most of the organization’s mind. Integrating process management is a vital reason in the quality management system. A robust quality management software is perfect for most of the medical device manufacturers along with the frequently complex...

Nov 25

Why factory resets are not sufficient to save your personal data?

One of the most vital steps for businesses is to keep your data safe in the internet era, where finks are active throughout the world to steal your data for their own purposes. It has also been noticed that one of the most critical steps in trading in mobile devices is to go through a […]...

Nov 25

What more about the Responsible Recycling scheme?

Responsible Recycling has emerged greatly in the past few years while the industry-wide standard is also spreading all over the world for controlling the disposal of e-waste. Getting R2 certification will teach you relevant practices and it will show the client your commitment to the protection of t...

Day: 14 July 2019