Quality Blog

Category: Factory Audits

12 Jul 2024

Combining ISO 13485 and ISO 14644 in an Audit

ISO 13485 and ISO 14644 are key standards that govern quality management systems and controlled environment conditions, respectively. […]

11 Jul 2024

How to Conduct ESG Audits? Detailed Checklist and Methods

An ESG audit evaluates a company’s environmental, social, and governance performance. It is a comprehensive way to ensure […]

02 Apr 2024

What is a Second-Party Audit?

In this article, Pro QC International provides a comprehensive overview of second-party audits. We explore their origins, the […]

27 Dec 2023

Supplier Audits: Everything You Need to Know

The importance of supplier audits cannot be overstated. They serve as a crucial backbone in maintaining the integrity, […]

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 […]

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