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.

AssurX Announces Migration to Switch for Cloud-Based QMS and Compliance Platforms
AssurX Announces Migration to Switch for Cloud-Based QMS and Compliance Platforms

AssurX Announces Migration to Switch for Cloud-Based QMS and Compliance Platforms

AssurX Blog2025-10-03T04:39:49+00:00August 19th, 2021|

Powerful Private Cloud Delivers Enterprise Performance and Security MORGAN HILL, [...]

How to Simplify CAPA Management with a Cloud-Based QMS
How to Simplify CAPA Management with a Cloud-Based QMS

How to Simplify CAPA Management with a Cloud-Based QMS

AssurX Blog2024-03-12T13:42:59+00:00July 13th, 2021|

Corrective and preventive action (CAPA) violations are the most frequently cited [...]

How COVID-19 Is Driving the Shift from Paper to Cloud QMS
How COVID-19 Is Driving the Shift from Paper to Cloud QMS

How COVID-19 Is Driving the Shift from Paper to Cloud QMS

AssurX Blog2021-06-16T06:37:17+00:00June 16th, 2021|

When COVID-19 hit in 2020, companies around the world suddenly found themselves [...]

Deviation vs. Nonconformance: What’s the Difference?
Deviation vs. Nonconformance: What’s the Difference?

Deviation vs. Nonconformance: What’s the Difference?

AssurX Blog2025-10-03T04:45:00+00:00June 8th, 2021|

Recent headlines over wasted COVID-19 vaccines reveal shocking instances of lab [...]

How to Meet New EU MDR Requirements for Vigilance and Reporting
How to Meet New EU MDR Requirements for Vigilance and Reporting

How to Meet New EU MDR Requirements for Vigilance and Reporting

AssurX Blog2024-01-13T02:07:39+00:00December 3rd, 2020|

After a one-year delay due to concerns over a shortage of notified bodies, the n [...]

Don’t take your foot off the gas on EU MDR implementation
Don’t take your foot off the gas on EU MDR implementation

Don’t take your foot off the gas on EU MDR implementation

AssurX Blog2020-04-03T15:31:23+00:00April 3rd, 2020|

The coronavirus has had a massive impact on the medical device industry. As a c [...]

The Six C’s of a Modern Complaint Management System 2020
The Six C’s of a Modern Complaint Management System 2020

The Six C’s of a Modern Complaint Management System 2020

AssurX Blog2020-03-10T07:15:08+00:00March 10th, 2020|

Regulators such as FDA, European Commission (EC), ISO 13485 require a product c [...]

Human Error is a Precipitator for Root Cause Analysis, Not Blame
Human Error is a Precipitator for Root Cause Analysis, Not Blame

Human Error is a Precipitator for Root Cause Analysis, Not Blame

AssurX Blog2024-06-03T13:33:05+00:00February 21st, 2020|

Have you ever been part of a process that had a failure or two? Perhaps you’ve b [...]

Assurx2020 Further Modernizes Efficiencies In Automating Quality Management
Assurx2020 Further Modernizes Efficiencies In Automating Quality Management

Assurx2020 Further Modernizes Efficiencies In Automating Quality Management

AssurX Blog2020-02-10T16:34:51+00:00February 10th, 2020|

Morgan Hill, CA., January 22, 2020, – AssurX, Inc., a leader in enterprise quali [...]

Configuration vs. Customization for Enterprise QMS Software
Configuration vs. Customization for Enterprise QMS Software

Configuration vs. Customization for Enterprise QMS Software

AssurX Blog2025-11-11T20:49:47+00:00January 23rd, 2020|

Experience shows that out-of-the-box configured software only works for business [...]