CQV
![Why Change Management is Important during CQV?](https://pharmadigests.com/wp-content/uploads/2023/10/900300-1.png)
Why Change Management is Important during CQV?
Change management is crucial in any Commissioning, Qualification, and Validation (CQV) activity within the pharmaceutical and other regulated industries for several important reasons: Robust change management helps ensure compliance, manage risks, maintain product quality, and facilitate efficient and controlled change implementation. It is an integral part of maintaining the quality, ... Read More
![Commissioning, Qualification, and Validation (CQV) in Pharmaceutical Industry](https://pharmadigests.com/wp-content/uploads/2023/10/900300.png)
Commissioning, Qualification, and Validation (CQV) in Pharmaceutical Industry
Commissioning, Qualification, and Validation (CQV) is one of the most important phases in achieving cGMP and regulatory compliance for a pharmaceutical manufacturing facility. CQV is a systematic approach to ensuring that facilities, equipment, and processes meet the required quality and regulatory standards. Each phase serves a specific purpose in the ... Read More