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Life Sciences
Preparing for ISO 13485 Harmonization: Where Do Things Stand Today?
In January 2024, the U.S. Food and Drug Administration (FDA) issued a final rule harmonizing its Quality System Regulat [...]
5 Places to Use a FMEA in Your Quality Process
Before any road trip, it makes sense to check your tire pressure along with levels of engine oil, windshield wiper flui [...]
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 – it’s essential. The ALCOA principles - [...]
Ways to Influence Stakeholder Buy-In During the CAPA Process
How can a quality manager secure stakeholder engagement and hold individuals accountable for the quality of their work [...]
CAPA is a Process, Not a Project: 3 Key Strategies for Success
The challenge of the quality manager is to convince stakeholders of their responsibilities and accountability in the CA [...]
Overcoming Deviations and Non-Conformances in Manufacturing: The Power of Automating Quality and Compliance
Manufacturers widely view process improvement frameworks like Lean as the solution to improving productivity and perfor [...]
