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.

11 11, 2025

Improving the Supplier Corrective Action Request Process with the QMS

By |2025-11-11T13:32:19+00:00November 11th, 2025|Archives, eMDR, FDA Regulated Industries, Food & Beverage Industry, Manufacturing Industries, Medical Device Industry, Pharmaceutical Industry, Quality Management, Regulatory Compliance Management, SaaS & Cloud Computing|

When I first started developing supplier quality management programs in pharma m [...]

4 11, 2025

AssurX Promotes Stephanie Ojeda to Vice President, Product Management, Life Sciences and Manufacturing

By |2025-11-04T18:49:46+00:00November 4th, 2025|FDA Regulated Industries, Manufacturing Industries, Medical Device Industry, Pharmaceutical Industry, Quality Management, Risk Management|

Reno, NV – November 4, 2025 – AssurX, a leading provider of quality management [...]

28 07, 2025

5 Essential Elements Shared by Leading Supplier Quality Management Systems

By |2025-07-28T16:33:25+00:00July 28th, 2025|FDA Regulated Industries, Food & Beverage Industry, Manufacturing Industries, Medical Device Industry, Pharmaceutical Industry, Quality Management, Regulatory Compliance Management, SaaS & Cloud Computing|

Global-scale events have tested the bounds of a supply chain system. The coronav [...]

23 07, 2025

Why Quality Audits Are Critical for Compliance in FDA and ISO Environments

By |2025-07-23T14:48:04+00:00July 23rd, 2025|Food & Beverage Industry, Manufacturing Industries, Medical Device Industry, Pharmaceutical Industry, Quality Management, Regulatory Compliance Management|

Quality audits are a cornerstone of compliance in FDA and ISO-regulated environ [...]

9 07, 2025

QMS Validation: How CSA Reduces Documentation Without Increasing Risk

By |2025-07-08T20:34:27+00:00July 9th, 2025|FDA Regulated Industries, Food & Beverage Industry, Manufacturing Industries, Medical Device Industry, Pharmaceutical Industry, Quality Management|

Documentation has long been at the heart of quality management system (QMS) val [...]

26 06, 2025

Supplier Scorecards vs. Spreadsheets: Risks of Manual Tracking

By |2025-06-26T14:08:20+00:00June 26th, 2025|Archives, eMDR, FDA Regulated Industries, Food & Beverage Industry, Manufacturing Industries, Medical Device Industry, Pharmaceutical Industry, Quality Management, Regulatory Compliance Management, SaaS & Cloud Computing|

Spreadsheets are usually the first tool used to manage suppliers, and the first [...]

17 06, 2025

QMS Software: When to Configure and When to Customize

By |2025-06-17T15:25:23+00:00June 17th, 2025|Archives, eMDR, FDA Regulated Industries, Food & Beverage Industry, Manufacturing Industries, Medical Device Industry, Pharmaceutical Industry, Quality Management, Regulatory Compliance Management, SaaS & Cloud Computing|

When it comes to managing quality and compliance in today’s regulated industries [...]

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