Pharma QMS: The Key Elements of QMS in Pharmaceuticals​

Pharma QMS: The Key Elements of QMS in Pharmaceuticals Ensuring Quality and Compliance Across Your Organization Did you know that a pharmaceutical company can receive misdemeanor fines that go up to 500,000 dollars and criminal fines that go up much higher, for FDA violations? In addition, they could also face delayed product launches and reputational […]

The Importance of CAPA in Quality Management Systems

Corrective and Preventative Action (CAPA) is a concept within the Food and Drug Administration’s (FDA) Good Manufacturing Practice (GMP). CAPA involves the systematic analysis of anomalies, defects, or inconsistencies in an attempt to prevent their recurrence.