Critical Aspects of Quality Management Systems: Focusing on the Validation Process
In regulated industries like pharmaceuticals, medical devices, and food manufac [...]
14
11, 2024
30
10, 2024
Preparing for ISO 13485 Harmonization: Where Do Things Stand Today?
In January 2024, the U.S. Food and Drug Administration (FDA) issued a final rul [...]
24
10, 2024
5 Places to Use a FMEA in Your Quality Process
Before any road trip, it makes sense to check your tire pressure along with lev [...]
9
10, 2024
The Role of Technology in Supporting ALCOA Principles: Strengthening Data Integrity in Life Sciences with Quality Management Software
In the highly regulated world of life sciences, data integrity is not optional [...]
29
08, 2024
Ways to Influence Stakeholder Buy-In During the CAPA Process
How can a quality manager secure stakeholder engagement and hold individuals ac [...]
22
08, 2024
CAPA is a Process, Not a Project: 3 Key Strategies for Success
The challenge of the quality manager is to convince stakeholders of their respo [...]
15
08, 2024
Overcoming Deviations and Non-Conformances in Manufacturing: The Power of Automating Quality and Compliance
Manufacturers widely view process improvement frameworks like Lean as the solut [...]
17
08, 2023
Aligning Incident Management with ISO 45001 Requirements
The number of ISO 45001 certificates is growing fast, jumping 54% from 2020 to 2 [...]
8
08, 2023
EHS Incident Management and Root Cause Analysis
Workplace safety incidents are a key driver of risk in manufacturing organizatio [...]
26
07, 2023
Risk Management in ISO 13485
In December 2023, the U.S. Food and Drug Administration (FDA) expects to issue i [...]
