CQV & CSV

As a natural process, Pharma facilities need to navigate though the Qualification & Validation cycles before a drug is produced. Commissioning, Qualification & Validation along with Computer System validation form an integral part of the Project delivery & Quality compliance. With our team of experts & partners we cover:

• Review of Validation Master Plan
• Developing CQV & CSV Plans
• Review Design Qualification of Systems
• System Level Impact Assessment
• Risk assessment
• Develop & Execute Protocols for IQ, OQ & PQ