Cell And Gene Therapy Analytics
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Explore The Analytics Knowledge Hub
5/22/2025
Discover smarter solutions with the new Analytics Knowledge Hub that provides articles, webinars, e-books, and infographics designed to enhance and streamline your bioprocess workflow.
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Rapid Micro Methods In QC Micro Testing: A NIBRT Perspective
5/29/2025
Learn about some of the advanced Rapid Micro Method systems that are being adopted by biopharma companies worldwide, and how they are changing the face of QC Microbiological testing.
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Maximize Quality Assurance Through Rapid Sterility Testing
9/10/2024
This webinar explores mitigating the risk of product loss, and production delays, as well as the critical role rapid sterility testing plays in ensuring the quality and safety of cell therapy products.
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Interview With Nico Chow And Sandi True, Field Applications Specialists
11/6/2025
Hear Nico Chow and Sandi True, Field Applications Specialists, discuss working with customers to help them evaluate and implement Residual DNA Quantitation, Mycoplasma Detection, and Microbial Identification Assays.
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Inside Bioprocessing: Multi-Omics
6/16/2025
Dive into multi-omics analysis with Paul Gulde, Chengjian Tu, and Femi Egbebi. In biopharmaceutical production, meeting the unique nutrient requirements of the cells is central to achieving optimal results.
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Innovative Strategies For Residual DNA And Viral Titre Quantitation
5/22/2025
Discover how digital PCR improves the accuracy of residual host cell DNA and viral titre quantification in biotherapeutic manufacturing to enhance product quality, safety, and regulatory compliance.
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Validation Of A qPCR Assay For Host Cell DNA Quantitation
6/9/2025
Here, we share the development and validation of a new, highly sensitive and accurate integrated solution for detection and quantitation of host cell DNA to help meet regulatory requirements.
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A Straightforward Path Toward Regulatory Compliance, Data Integrity, And Computer Systems Validation
6/9/2025
Learn practical strategies for validating microbial identification systems in cGMP. Understand regulatory guidance and master a complete Computer Systems Validation plan for full compliance.
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Rapid Process Development And Technical Support For AAV Scaleup
12/17/2024
Accelerate your AAV production journey. Learn how rapid process development and expert support can streamline your path from vial to purified bulk, ensuring scalable and efficient manufacturing.
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Introducing The Applied Biosystems Resdnaseq Quantitative DNA System
11/20/2025
Thermo Fisher Scientific's portfolio of resDNASEQ solutions is here to meet your specific needs enabling you to test for residual host cell DNA and release your biotherapeutics with confidence in safety and confidence in product quality.