Top 5 QHSE Benefits that can turn your workplace Better
Wali Alam
8 April 2022
A QHSE management system helps to promote the sustainability of an organization by making sure that the health & safety
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A Guide to FDA CAPA Requirements and Management
Wali Alam
29 January 2022
Corrective and Preventive Action (CAPA) is a fundamental part of an effective quality management system. For companies operating in FDA-regulated
Why is CAPA Management Important?
Wali Alam
27 January 2022
CAPA (Corrective and Preventive Action) forms the basis of any Quality Management system. It is an essential part of the
What is CAPA Management? (ISO standard)
Wali Alam
16 January 2022
CAPA is the acronym for Corrective and Preventive Action. CAPA’s planning, organizing, directing, and control is called CAPA management. CAPA
Using Trend Analysis to Control Quality Nonconformances
Rayeed Rahman
28 December 2021
Why am I continually writing the same nonconformance reports, over and over? Multiple types of organizations utilize trend analysis to gauge their
What is a Non-Conformance Management System?
Wali Alam
4 December 2021
In our previous article, we delved into what Nonconformance was and what Non-Conformance Management Software did to the whole process of managing
Nonconformance Management for FDA and ISO Compliance
Wali Alam
4 December 2021
Nonconformance management should consist of procedures that allow an organization to identify, segregate, evaluate, document, and dispose of output that
What are examples of ISO audit non-conformances?
Wali Alam
3 December 2021
What does the standard require? As quality professionals, we are all familiar with manufacturing non-conformances. Operational irregularities, wrong sizes, colors,
Maintenance Management in QMS Software
Rayeed Rahman
31 March 2021
The maintenance practices and technologies have developed to meet the needs of the developing industrial environment. The purpose has evolved
All things CAPA in IS0-9001 standards
Wali Alam
31 March 2021
Every organization has its share of problems: customer complaints, process defects, faulty components, misleading data or reports, and a plethora of