There’s a great deal of common ground between continued process verification (CPV) and annual product quality review (APQR), yet these programs are often managed separately resulting in redundant activities. Integrating CPV and APQR with a unified data infrastructure, advanced techniques and tools for automating data collection, analysis, and reporting will significantly improve operational performance. In this webinar, we will focus on how automation enhances efficiency, accuracy, and compliance while reducing manual effort. Industry experts will share insights on implementing a robust and integrated CPV and APQR frameworks effectively.
In this webinar, you will learn:
- How to integrate CPV and APQR
- Advanced techniques to integrate data sources to enable CPV and APQR automation
- Digital tools for streamlined quality management
- How to enhance regulatory compliance
Speaker

Shitanshu Srivastava
Merck
Global Lead, Implementation and Support of Analytics Solutions
Shitanshu Srivastava leverages his industry knowledge and expertise in data acquisition and analytics to design and implement digital solutions for complex pharma and biopharma manufacturing processes at Merck. Previously, he served as manufacturing science and systems manager at Dr. Reddy’s Laboratories and as senior product application and business development manager at the software startup, Simplyfeye. Shitanshu holds a Bachelor of technology in biotechnology from Vellore Institute of Technology.
Pharma and biopharma manufacturing
- Pharma and biopharma manufacturing
期间:1h
语言:English
场次 1:往期 September 19, 2024
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