CSV: Leveraging Advanced Technologies and Learnings from Pharma 4.0
Explore how leveraging technologies across pharmaceutical development and manufacturing processes will help pharma life sciences companies address challenges and achieve a future state faster. In this webcast, sponsored by RAPS, Bryan Ennis and David Hall Rode discuss the future state of technology across pharmaceutical manufacturing and the challenges companies will face. They review what’s going to be required and how life sciences companies can best position themselves – from predictive maintenance to validation requirements – to adopt transformational technologies and drive business value.
Featured Resources
The convergence of AI and Quality Management marks a paradigm shift in how Life Sciences organizations meet their GxP obligations. Examine key challenges—from compliance complexities and validation demands to talent shortages and risk management concerns.
Read the WhitepaperAs the life sciences landscape rapidly evolves, technology adoption demands agile validation methods to maintain GxP compliance. Learn how organizations can shift from project-based validation to a process-driven approach, integrating validation into their Quality Management System.
Read the WhitepaperManual computer software validation processes cost life sciences organizations up to 30% in additional project budget. As companies struggle to keep up with a surge of app and software integrations, they incur validation debt: the mounting cost of stretched resources, blanket testing, and missed GxP requirements.
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