Accelerating INDs Without Animals: How CROs Can Capitalize on FDA’s New Methodologies
The FDA direct final rule officially clears the path for organs-on-chips and in vitro models. Advanced CROs can capture the shifting outsourcing market
Advertisement
Biotechnology & Life Science Products Articles
Advertisement
Psilocybin Potency Testing: Ensuring Quality and Safety of Magic Mushrooms
Psilocybin potency testing is an essential step in ensuring the safety, quality, and efficacy of psilocybin products.
Sterility Testing Guide: USP <71>, Direct Inoculation vs. Membrane Filtration, and B&F Validation
Laboratories must perform sterility testing to ensure that products are contaminant free
What Is Laboratory Turnaround Time (TAT)?
Learn the phases, STAT vs. routine benchmarks, what affects TAT in contract testing, and how to specify TAT requirements when outsourcing lab work
The Kirby-Bauer Disk Diffusion Test: Complete Guide to Method, Interpretation, and Applications
Simplicity, reliability, and an ability to guide antimicrobial therapy make it an essential technique for both clinical and research laboratories.
Pharmaceutical Drug Development: Small Molecules, Large Molecules, and the New Modalities
Researchers, developers, and manufacturers should be able to leverage the unique advantages of both small and large molecule approaches to address unmet medical needs
Next-Generation Sequencing (NGS): Transformative Applications and Laboratory Outsourcing Strategies
NGS is standard practice, but infrastructure is costly. Here is why life science firms outsource it to accredited testing labs
Biological Activity Reaction Test (BART): A Comprehensive Guide
While BART has some limitations, its benefits make it a valuable addition to water management and environmental testing industry
Outsourcing GLP-1 Analysis: Lab Methods for API Purity and Sterility
What are the exact testing protocols compounding pharmacies need to confidently release weight-loss injectables? How to find the right contract lab to run them?
Navigating the Green vs. Clean Dilemma in Medical Device Manufacturing
How med-tech manufacturers are leveraging smarter material engineering and laboratory validation to hit sustainability targets without failing the FDA audit
Optimizing the DMTA Cycle: Closing the Gap Between AI and Pharma R&D
Manual data translation limits AI, but connecting the DMTA cycle turns scattered data into actionable knowledge
Advertisement
Advertisement