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LOGIN
1-888-927-7879 | 1-408-778-1376

LOGIN | 1-888-927-7879 | 1-408-778-1376

corrective and preventive action

5 03, 2024

Top Considerations for Compliance Management Tools
Top Considerations for Compliance Management Tools

Top Considerations for Compliance Management Tools

By Stephanie Ojeda|2025-03-18T09:27:36+00:00March 5th, 2024|Audit Management, Corrective Action (CAPA), Document Management, FDA Regulated Industries, Food & Beverage Industry, Medical Device Industry, Pharmaceutical Industry, Quality Management|

Implementing an automated compliance management solution is a mammoth undertakin [...]

17 08, 2023

Aligning Incident Management with ISO 45001 Requirements
Aligning Incident Management with ISO 45001 Requirements

Aligning Incident Management with ISO 45001 Requirements

By Stephanie Ojeda|2025-03-18T09:29:45+00:00August 17th, 2023|Energy & Utilities Industry, Food & Beverage Industry, Manufacturing Industries, Medical Device Industry, Quality Management|

The number of ISO 45001 certificates is growing fast, jumping 54% from 2020 to 2 [...]

30 05, 2023

Complaint Management for Life Sciences with an Automated QMS
Complaint Management for Life Sciences with an Automated QMS

Complaint Management for Life Sciences with an Automated QMS

By Stephanie Ojeda|2025-05-07T23:01:07+00:00May 30th, 2023|Complaint Management, Document Management, Manufacturing Industries, Medical Device Industry, Quality Management|

Effective complaint handling is fundamental to life sciences quality management [...]

21 10, 2021

How to Use the 8D Method for Investigations
How to Use the 8D Method for Investigations

How to Use the 8D Method for Investigations

By Sal Lucido|2023-12-05T14:50:19+00:00October 21st, 2021|FDA Regulated Industries, Manufacturing Industries, Medical Device Industry, Pharmaceutical Industry, Quality Management, Regulatory Compliance Management, Risk Management|

Each day, quality leaders run across all types of problems. Fortunately, some ca [...]

1 09, 2021

Root Cause Analysis and CAPA: Creating a Closed-Loop Process
Root Cause Analysis and CAPA: Creating a Closed-Loop Process

Root Cause Analysis and CAPA: Creating a Closed-Loop Process

By AssurX Blog|2024-12-31T23:23:15+00:00September 1st, 2021|FDA Regulated Industries, Food & Beverage Industry, Manufacturing Industries, Medical Device Industry, Pharmaceutical Industry, Quality Management|

This article examines why a closed-loop root cause analysis (RCA) and corrective [...]

11 12, 2019

Looking Ahead: 2020 Life Sciences Technology Trends
Looking Ahead: 2020 Life Sciences Technology Trends

Looking Ahead: 2020 Life Sciences Technology Trends

By AssurX Blog|2025-04-04T02:14:25+00:00December 11th, 2019|Document Management, eMDR, FDA Regulated Industries, Manufacturing Industries, Medical Device Industry, Pharmaceutical Industry, Quality Management, Regulatory Compliance Management, Risk Management, Uncategorized|

The Life Sciences industry has always been fast-paced and competitive. Changes [...]

21 10, 2019

Advanced Medical Solutions Selects AssurX Quality Management and Regulatory Compliance Software
Advanced Medical Solutions Selects AssurX Quality Management and Regulatory Compliance Software

Advanced Medical Solutions Selects AssurX Quality Management and Regulatory Compliance Software

By AssurX Blog|2023-09-28T21:31:13+00:00October 21st, 2019|AssurX News + Success Stories, FDA Regulated Industries, Manufacturing Industries, Quality Management, Regulatory Compliance Management|

AssurX Platform will Automate and Standardize Quality Operations in the UK, Neth [...]