eBooks
Introduction to tangential flow filtration (TFF)
A practical eBook to biomolecule separation, concentration & diafiltration
Decentralised Clinical Trials In The EU
DCTs can take a variety of forms depending on patients’ needs, study protocol, drug company preferences, or regulatory requirements.
Rapid and Efficient Measurement of Critical Quality Attributes
Critical quality attributes (CQAs) are defined as a physical, chemical, biological, or microbiological property or characteristics that should be within an appropriate limit, range, or distribution to ensure the desired product quality.
A Compendium for Successful BLI and SPR Assays: Octet® Label-Free Biosensor Analysis
Designing and performing assays that accurately measure the binding kinetics of biomolecular interactions can seem too specialized and out of reach for many researchers.
A Compendium for Successful BLI and SPR Assays
The field of real-time, label-free protein binding analysis has historically been marked with steep learning curves.
Choose the Optimum Pipette and Be Connected for the Future
Pipettes play a critical role in the laboratory, as they are essential for the accurate delivery of samples and reagents in a wide range of experiments. Laboratories are facing increasing pressure to increase throughput, which has led to greater demand for pipettes that can facilitate more efficient workflows.
Welcome to the Future of Live-Cell Analysis
This comprehensive guide introduces cutting-edge technologies that are transforming the field!
Leveraging Advanced Analytical Tools to De-risk Pharmaceutical Development
Drug development continues to advance understanding about causes of disease, as well as to innovate therapeutic modalities.
How Optimized Equipment Cleaning Accelerates Validation and Time to Market
Validated equipment cleaning is essential for compliant biopharma manufacturing but too often it becomes a bottleneck that slows changeovers, increases residue‑related failures, and complicates validation.
Accelerate Drug Development with Innovative 360° CDMO and CRO Solutions
As R&D costs continue to rise and timelines extend, biotech and pharmaceutical companies are under increasing pressure to deliver therapies faster and more efficiently. Achieving right-first-time outcomes and reducing development risks have become essential priorities across the industry.
