Blog Post

Take a break and read all about it

Reducing Nonconformances
Blog Post

Reducing Nonconformances

Reducing nonconformances in an organization is fairly easy to do, although it is impossible to eliminate them completely. It is however always better to prevent issues rather than reacting to them.

Construction Nonconformances
Blog Post

Construction Nonconformance

A construction quality control plan should contain a systematic process that can be used to manage construction nonconformances, whether they’re simple or difficult.

Manufacturing Nonconformances
Blog Post

Manufacturing Nonconformances

Manufacturing nonconformances are products that don’t meet specifications established by regulators or manufacturers. Nonconformances are however not only defective physical products.

nonconformance report
Blog Post

How to Create a Nonconformance Report

Creating a nonconformance report is not that difficult. The 7 steps described in this article will go a long way in helping you write a report that will form an integral part of your company’s continual improvement process.

Causes of ISO 9001 Non-Conformance
Blog Post

What Are the Most Common Causes of ISO 9001 Non-Conformance?

Causes of ISO 9001 non-conformance can vary from things like lack of employee training, inadequate management commitment, ineffective process controls, insufficient documentation, resistance to change, and poor communication.

Kaizen Continuous Improvement
Blog Post

Kaizen Continuous Improvement

Fundamental to Kaizen continuous improvement is the philosophical belief that everything can be improved. When using this approach, incremental changes gradually add up to substantial changes over the long term.

PDCA cycle
Blog Post

PDCA Cycle

he Plan-Do-Check-Act (PDCA) cycle is a scientific method for iterative problem-solving that is used to continuously improve products and processes by identifying improvement opportunities. It is also referred to as the Shewhart cycle or the Deming cycle.

capa records
Blog Post

CAPA Records – The CAPA Process Explained

CAPA records and the CAPA process is often a big issue for ISO 9001-accredited companies. CAPA (corrective and preventive action) still remains one of the most cited areas for external audits during ISO QMS audits.

Do You Want To Boost Your Business?

drop us a line and keep in touch