(888) 507-0619
sales@qi-a.com
QISS QMS
Document Control
Audit Management
Supplier Management
Nonconformance Management
Corrective and Preventive Action
Root Cause Analysis
Calibration Management
Maintenance Management
Training Management
Customer Satisfaction Survey
Customer Complaint
Health and Safety Management System
Risk Management
Risk Prevention
Management of Change
HSE Reporting
Engineering Change Request
Business Solutions
Web Based Software
Quality Management System (QMS)
Expanded Management System
Health and Safety Mgmt System
Large Manufacturing
Pharma & Medical Devices
Comprehensive Management System
Small Enterprise
QISS Software Applications
Environmental Management Modules
Core QHSE Management System
Medium Size Manufacturing
Environmental Management System
Video
Audit
Calibration
CAPA
Customer Management
Document Management
QISS Software
Maintenance
MOC
Risk Management
Supplier Management
Knowledge Management
Training Video
Management Review
NCR
Training
ECR/ECN
HSE
Training
Developing and Implementing a NEW ISO 9001:2015
Internal and Supplier Auditing of QMS
TRANSITIONING from ISO 9001:2008 to ISO
Learning Center
About Us
About Us
Auditing
Consulting
Training
Get Demo
Quality
Home
Learning Center
Quality
Latest Post
Building Security with Accounting Software (Audit Management)
22 January, 2023
The Benefits of an Electronic Quality Management System
17 October, 2022
Why You Should Implement a Document Control System?
19 December, 2022
ISO and Document Control (ISO 9001:2015)
05 February, 2021
What are the CAPA process steps in Quality Management?
28 January, 2022
Categories
Quality
Supplier
QHSE
Tags
Quality
What are the benefits of CAPA Management Software?
16 January, 2022
Wali Alam
To understand CAPA Management Software’s benefits, we would need to understand what CAPA Management Software is.
Continue Reading
Quality
What is CAPA Management? (ISO standard)
16 January, 2022
Wali Alam
CAPA is the acronym for Corrective and Preventive Action. CAPA’s planning, organizing, directing, and control is called CAPA management.
Continue Reading
Quality
What is a Non-Conformance Management System?
04 December, 2021
Wali Alam
In our previous article, we delved into what Nonconformance was and what Non-Conformance Management Software
Continue Reading
Quality
Nonconformance Management for FDA and ISO Compliance
04 December, 2021
Wali Alam
Nonconformance management should consist of procedures that allow an organization to identify, segregate, evaluate, document, and dispose of output.
Continue Reading
Quality
Benefits of Nonconformance Management Software
03 December, 2021
Wali Alam
The quality, safety, and reliability of your products depend on your ability to conform to specifications. When a nonconformance occurs, it is essential to resolve it efficiently, timely and remain compliant with corresponding standards.
Continue Reading
‹
1
2
3
4
5
6
7
8
9
›