Bioanalytical insights, straight from the lab

Technical Resources &
Thought Leadership

Our mission doesn’t stop at the bench. We publish practical, experience-backed content to help our partners navigate evolving regulations, explore emerging trends and accelerate timelines. Dive into our reports, resources and behind-the-scenes perspectives from the front lines of regulated bioanalysis.

LC–MS/MS of Semaglutide & Tirzepatide

This poster presents Veloxity’s LC–MS/MS methods for quantifying semaglutide and tirzepatide in plasma and brain tissue. Explore data demonstrating low-ng/mL sensitivity, reproducible quantitation and reliable performance across matrices.

GLP-1 & Peptide Bioanalysis Brochure

See how Veloxity supports peptide and GLP-1 receptor agonist (RA) programs with proven LC–MS/MS methods, low-nM sensitivity and rapid turnaround. Our brochure highlights our experience, selectivity and speed—showing how we deliver reliable, on-schedule results across study phases.

Accelerating Drug Development Along the Entire Lifecycle

Drug programs can lose weeks to slow bioanalysis, siloed handoffs and documentation gaps. This report shows how to align LC–MS/MS to the next phase from day one—moving seamlessly from discovery through GLP and into clinical. You’ll get practical checklists, “tips & traps,” real-world snapshots and sponsor perspective from our guest co-author, industry veteran, Andy Vick, PhD, BlueWater Biosciences. Ideal for teams aiming to combine speed with scientific rigor under GLP/GCP and ICH M10 expectations.

VELO: A Custom Lab Operations System

Veloxity Labs built VELO, a custom LQMS that unifies workflows, speeds timelines, ensures data integrity, and delivers clear client communication. Download our report to learn more.

Overcoming Challenges in Rare Disease Therapeutic Development

Download this report to learn how bioanalytical partners can accelerate high-complexity programs with small samples and high stakes.

GCP Considerations in the Bioanalytical Laboratory: Why it Matters

The newly released 2025 FDA Biomarker Guidance marks a step forward in biomarker bioanalysis regulation. Download our report to learn more.