Quality Blog

Category: Factory Audits

10 Oct 2023

Does IATF 16949 Require a Supplier Audit?

At its core, IATF 16949 emphasizes continuous improvement, defect prevention, and the reduction of variations and waste in […]

29 Jun 2023

Forced Labor Compliance and Detection in SA8000 Audits

Identifying Forced Labor with third-party SA8000 Audits Forced labor has become an unfortunate yet pervasive issue, deeply embedded […]

15 Jun 2023

How to Prepare for an FDA Inspection of Your Medical Device QMS

An FDA inspection of a medical device company’s quality management system (QMS) can be a daunting experience. However, […]

09 Mar 2023

Raising the Bar on Furniture Quality with Manufacturing Process Audits

The furniture industry is a highly competitive market, with manufacturers constantly looking for ways to improve product quality, […]

22 Dec 2022

How to combine an MDR 2017/745 and an ISO 13485 Supplier Audit

MDR (EU) 2017/745 is a set of regulations that govern the European medical device market. It was created […]

22 Dec 2022

What is Medical Device Single Audit Program (MDSAP)?

Medical Device Single Audit Program (MDSAP) An MDSAP is a type of audit that focuses on the medical […]

20 Jun 2022

Evaluating potential suppliers with Supplier Quality Audits

What is a Supplier Quality Audit? A supplier quality audit is a general assessment of the supplier’s operation […]

11 Nov 2021

Selecting the right social compliance standard

Auditing a new supplier against social compliance standards is a must. Such an audit ensures that the business […]

30 Jul 2021

How to Ensure Social Compliance Using SA8000 and Other HSE Audits

Social compliance issues have been a growing concern for several years now and only continue to rise as […]

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