FOR PHARMA & BIOTECH R&D
Reproducible results. Across every bench, every site.
Clarida standardizes your qPCR analysis workflow so every scientist in your team gets the same answer from the same data - without the spreadsheet chaos.
Sound familiar?
- Dozens of qPCR experiments per week, each scientist with their own Excel template, their own normalization approach, their own outlier flagging.
- Results don't match across sites. You can't tell if discrepancies are biology or methodology.
- QC checks are manual and inconsistent. Problems propagate for months before anyone notices.
- Onboarding a new scientist takes weeks of "this is how we do it here."
- Re-analyzing last quarter's data with different reference genes? Good luck finding the original files.
Why Clarida
One standard, every scientist
Define analysis parameters once. Every experiment follows the same normalization, outlier criteria, and QC thresholds. No analyst-dependent variation.
QC that catches problems before they propagate
Batch-to-batch variation, cDNA synthesis consistency, plate homogeneity - Clarida flags issues at source, not after three months of downstream work.
Team-wide visibility
See every experiment, every result, every decision. When someone leaves the team, their work doesn't leave with them.
Scale without sacrificing rigor
Whether 10 experiments a month or 200, the workflow stays the same. Add team members without retraining overhead.
Built on geNorm and MIQE
The same scientific standards that underpin your SOPs - built into the software, not bolted on.
Key use cases
Explore how Clarida handles specific scientific questions.
Credits-based model that scales with your team. One budget, flexible allocation across experiments, QC, and advanced analysis. Enterprise pricing for large teams.
Ready to get started?
Free to start. No credit card. Enterprise plans available for large teams.