Discover an insightful webinar focused on the importance of data integrity in biopharmaceutical manufacturing and the selection of analytical instruments.
Data integrity is the cornerstone of ensuring drug safety, efficacy and quality. Discover how an osmometer can enhance manufacturing processes and help ensure regulatory compliance by maintaining robust data integrity. Selecting analytical instruments that prioritize data integrity is essential for safeguarding product quality and compliance. By implementing proactive data integrity measures, errors can be prevented, remediation efforts can be reduced and a compliance-focused culture can be built.
The expert speakers will showcase how osmolality testing is used to monitor product batches, ensuring quality across various workstreams. The advanced technology helps ensure accurate and reliable data, which is crucial for maintaining high standards in biopharmaceutical manufacturing. The integrity of the data generated plays a vital role in the consistent monitoring and quality assurance of biopharmaceutical products.
Don’t miss this opportunity to gain practical strategies for ensuring compliance, quality and data integrity in biopharmaceutical manufacturing by choosing the right analytical instruments. Embrace the importance of data integrity to drive excellence in manufacturing processes.
Register for this webinar today to explore how robust data integrity practices and the right analytical tools can transform the biopharmaceutical manufacturing processes.
Speakers

Sachin Patel, Associate Director of QC Systems, Biogen
Sachin Patel is the Associate Director of QC Systems at Biogen. His team oversees the lifecycle management and maintenance activities for several analytical instrument and equipment systems across Global Quality Control and Manufacturing areas.
Over his 20+ year career in the pharma and biotech space, he has grown fond of using technology and sound problem-solving skills to support resolution for compliance gaps across business areas. In his free time, he enjoys playing basketball, traveling to new place and spending time with his family and friends.

Shweta Nair, Director, Biopharma Osmometer Portfolio, Advanced Instruments
Shweta Nair is the Director of the Biopharma Osmometer Portfolio at Advanced Instruments, bringing over a decade of experience in the biopharma and life sciences industries. Since 2019, she has led the development and launch of innovative osmometer products, focusing on improving accuracy, reliability and data integrity in osmolality testing.
She stays actively engaged with industry experts, regulatory bodies and associations to keep up with evolving standards and best practices. Before joining Advanced Instruments, Shweta was a Global Product Manager at Millipore Sigma, where she managed lab equipment for biopharma and research applications.
Who Should Attend?
This webinar will appeal to those working in the following areas or having the following job titles:
- Biopharmaceutical manufacturing professionals
- Quality Assurance and Control Specialists
- Regulatory Compliance Officers
- Data integrity and lifecycle management experts
- Research and development scientists
What You Will Learn
Attendees will learn about:
- Why data integrity is crucial for ensuring drug safety, efficacy and quality in biopharmaceutical manufacturing
- How an osmometer can enhance manufacturing processes and ensure regulatory compliance by maintaining robust data integrity
- How implementing proactive data integrity measures can prevent errors, reduce remediation efforts and foster a compliance-focused culture
- A case study showcasing how osmolality testing ensures quality across various workstreams and maintains high standards in biopharmaceutical manufacturing
Xtalks Partner
Advanced Instruments
Advanced Instruments is a global company offering a novel portfolio of analytical tools, including OsmoTECH®, a robust line of micro-osmometers to support bioprocessing and quality control (QC), and Solentim, a portfolio of best-in-class imaging and single-cell deposition technologies for cell line development workflows and assurance of clonality for regulatory bodies.
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