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.

5 Ways an EQMS Resolves Change Management and Change Control Pains
5 Ways an EQMS Resolves Change Management and Change Control Pains

5 Ways an EQMS Resolves Change Management and Change Control Pains

Sal Lucido2024-06-03T13:58:34+00:00June 21st, 2022|

In the life science industry, adjustments are a necessary element throughout the [...]

Understanding FDA Alignment of ISO 13485 with Quality System Regulation
Understanding FDA Alignment of ISO 13485 with Quality System Regulation

Understanding FDA Alignment of ISO 13485 with Quality System Regulation

AssurX Blog2024-03-04T21:30:05+00:00April 20th, 2022|

The FDA’s official proposal to align its Quality System Regulation (QSR) with IS [...]

miraDry Implements AssurX Quality Management and Regulatory Compliance Software
miraDry Implements AssurX Quality Management and Regulatory Compliance Software

miraDry Implements AssurX Quality Management and Regulatory Compliance Software

Tracy Orlick2025-10-03T04:17:01+00:00March 31st, 2022|

MORGAN HILL, CA, UNITED STATES, March 31, 2022 – AssurX, Inc. (AssurX), a leade [...]

How an EQMS can Reduce CAPA and Complaint Observation Trends
How an EQMS can Reduce CAPA and Complaint Observation Trends

How an EQMS can Reduce CAPA and Complaint Observation Trends

AssurX Blog2025-05-07T23:13:18+00:00March 31st, 2022|

As we move through 2022, we look forward to new opportunities, new challenges, [...]

5 Tips for Turning GMP Audits from an Adversarial to a Cooperative Process
5 Tips for Turning GMP Audits from an Adversarial to a Cooperative Process

5 Tips for Turning GMP Audits from an Adversarial to a Cooperative Process

Sal Lucido2022-03-24T07:27:10+00:00March 24th, 2022|

This article is part two of a two-part series focused on GMP quality audit manag [...]

Remote Quality Audits for Regulated Companies Come of Age
Remote Quality Audits for Regulated Companies Come of Age

Remote Quality Audits for Regulated Companies Come of Age

Sal Lucido2025-01-01T00:01:28+00:00March 17th, 2022|

This article is part one of a two-part series focused on GMP quality audit mana [...]

How to Conduct Remote Supplier Quality Audits in a QMS
How to Conduct Remote Supplier Quality Audits in a QMS

How to Conduct Remote Supplier Quality Audits in a QMS

AssurX Blog2022-03-08T14:47:33+00:00March 3rd, 2022|

Since the Covid pandemic, regulators and notified bodies have been doing more re [...]

Trend Watch: 2022 and Beyond Will see Maturation of Internal Control Programs
Trend Watch: 2022 and Beyond Will see Maturation of Internal Control Programs

Trend Watch: 2022 and Beyond Will see Maturation of Internal Control Programs

Kathryn Wagner2024-07-16T22:55:59+00:00February 24th, 2022|

Technology, Politics, Climate, and the Coronavirus will Drive Maturation of Int [...]

7 Benefits of Quality Risk Management in the EQMS
7 Benefits of Quality Risk Management in the EQMS

7 Benefits of Quality Risk Management in the EQMS

Sal Lucido2024-03-04T21:20:32+00:00February 9th, 2022|

Regulators and standards organizations are increasingly requiring manufacturers [...]

5 Reasons Why an Enterprise Quality Management System (EQMS) is Imperative
5 Reasons Why an Enterprise Quality Management System (EQMS) is Imperative

5 Reasons Why an Enterprise Quality Management System (EQMS) is Imperative

Sal Lucido2024-03-04T21:16:46+00:00January 13th, 2022|

Many companies are still clinging to paper-based and unconnected electronic proc [...]