Introduction
In this webinar our experts Kieran Evans and Valentina Paolucci discuss analytical methodologies using UV-Vis techniques. Pharmaceutical testing labs need the flexibility to perform a wide range of analyses, from analytical method development for QA/QC to basic research into new drug candidates to dissolution testing. The LAMBDA 365+ is adaptable to all these applications, as well as being 21 CFR Part 11 compliant to meet your most stringent government and industry regulations.
Learning Outcomes:
- USP method compliance
- Solvent analysis
- DNA melting experiments
- Enzyme kinetics
- Biomolecule and biomedical implant characterization
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