Pharmaceutical Industry

The “Pharmaceutical Industry” category at AssurX focuses on addressing challenges and opportunities within the sector. This section provides insights into quality management, regulatory compliance, and process optimization for drug development and manufacturing. It emphasizes ensuring product safety and efficacy. Discover strategies to navigate complex regulations and enhance operational efficiency. AssurX offers tools and knowledge to help pharmaceutical professionals maintain compliance, improve quality, and drive innovation.

21 05, 2025

Human Factors in CAPA Part III: How To Secure Management Commitment
Human Factors in CAPA Part III: How To Secure Management Commitment

Human Factors in CAPA Part III: How To Secure Management Commitment

By Stephanie Ojeda|2025-05-21T13:32:55+00:00May 21st, 2025|FDA Regulated Industries, Food & Beverage Industry, Manufacturing Industries, Medical Device Industry, Pharmaceutical Industry, Quality Management|

In the third and final part of our Human Factors in CAPA series, we’re tackling [...]

14 05, 2025

Human Factors in CAPA Part II: How to Improve CAPA Accountability
Human Factors in CAPA Part II: How to Improve CAPA Accountability

Human Factors in CAPA Part II: How to Improve CAPA Accountability

By Stephanie Ojeda|2025-05-19T18:44:35+00:00May 14th, 2025|FDA Regulated Industries, Food & Beverage Industry, Manufacturing Industries, Medical Device Industry, Pharmaceutical Industry, Quality Management|

In Part I of our Human Factors in CAPA series, we talked about employee engagem [...]

7 05, 2025

Human Factors in CAPA Part I: How to Improve Employee Engagement
Human Factors in CAPA Part I: How to Improve Employee Engagement

Human Factors in CAPA Part I: How to Improve Employee Engagement

By Stephanie Ojeda|2025-05-07T15:05:26+00:00May 7th, 2025|FDA Regulated Industries, Food & Beverage Industry, Manufacturing Industries, Medical Device Industry, Pharmaceutical Industry, Quality Management|

At its core, corrective and preventive action (CAPA) is about systematically ev [...]

17 04, 2025

Mastering the 8D Problem-Solving Methodology: A Guide to Root Cause Analysis in Manufacturing
Mastering the 8D Problem-Solving Methodology: A Guide to Root Cause Analysis in Manufacturing

Mastering the 8D Problem-Solving Methodology: A Guide to Root Cause Analysis in Manufacturing

By Stephanie Ojeda|2025-04-17T12:50:31+00:00April 17th, 2025|FDA Regulated Industries, Food & Beverage Industry, Manufacturing Industries, Medical Device Industry, Pharmaceutical Industry, Quality Management|

Every day, quality leaders face a variety of production and process issues. Whi [...]

24 03, 2025

Understanding the Differences Between Deviation vs. Nonconformance
Understanding the Differences Between Deviation vs. Nonconformance

Understanding the Differences Between Deviation vs. Nonconformance

By Stephanie Ojeda|2025-04-04T02:10:09+00:00March 24th, 2025|Deviation, FDA Regulated Industries, Manufacturing Industries, Medical Device Industry, Pharmaceutical Industry, Quality Management, Regulatory Compliance Management|

The pharmaceutical industry and the medical device industry have unique ways of [...]

13 03, 2025

How to Use a Risk Matrix to Ensure Effective Risk Management
How to Use a Risk Matrix to Ensure Effective Risk Management

How to Use a Risk Matrix to Ensure Effective Risk Management

By Stephanie Ojeda|2025-05-07T15:08:38+00:00March 13th, 2025|FDA Regulated Industries, Manufacturing Industries, Medical Device Industry, Pharmaceutical Industry, Quality Management, Regulatory Compliance Management, Risk Management|

In manufacturing and in life, we can never completely eliminate risk. What matt [...]

10 03, 2025

3Analytics Partners With AssurX to Revolutionize IMDRF Coding Using AI
3Analytics Partners With AssurX to Revolutionize IMDRF Coding Using AI

3Analytics Partners With AssurX to Revolutionize IMDRF Coding Using AI

By Tamar June|2025-03-18T08:55:18+00:00March 10th, 2025|FDA Regulated Industries, Manufacturing Industries, Medical Device Industry, Pharmaceutical Industry, Quality Management, Risk Management|

The IMDRF Coding solution integrates seamlessly into AssurX EQMS, ensuring comp [...]

27 02, 2025

Enhancing Compliance Through Quality Risk Management
Enhancing Compliance Through Quality Risk Management

Enhancing Compliance Through Quality Risk Management

By Stephanie Ojeda|2025-03-18T08:56:54+00:00February 27th, 2025|FDA Regulated Industries, Manufacturing Industries, Medical Device Industry, Pharmaceutical Industry, Quality Management, Regulatory Compliance Management, Risk Management|

Quality risk management (QRM) has become a crucial tool for ensuring regulatory [...]

6 02, 2025

BPM Partners with AssurX to Enhance Cybersecurity and Compliance Solutions for Energy and Utility Industry
BPM Partners with AssurX to Enhance Cybersecurity and Compliance Solutions for Energy and Utility Industry

BPM Partners with AssurX to Enhance Cybersecurity and Compliance Solutions for Energy and Utility Industry

By AssurX Blog|2025-03-18T08:57:38+00:00February 6th, 2025|FDA Regulated Industries, Manufacturing Industries, Medical Device Industry, Pharmaceutical Industry, Quality Management, Risk Management|

SAN FRANCISCO, Jan. 15, 2025 – BPM LLP, one of the 35 largest public accounting [...]

28 01, 2025

Implementing Global Data Privacy Compliance Plans
Implementing Global Data Privacy Compliance Plans

Implementing Global Data Privacy Compliance Plans

By Paul Fricke|2025-04-04T02:25:00+00:00January 28th, 2025|FDA Regulated Industries, Manufacturing Industries, Medical Device Industry, Pharmaceutical Industry, Quality Management, Risk Management|

As businesses continue to embrace digital transformation, cloud computing has e [...]