Our strategic and comprehensive approach has driven innovations from the lab bench to patient care, creating significant impacts for patients.
Protocol-Plus
Achieve Reliable & Reproducible
Experiment Results
An AI-powered platform guiding scientists through every step of an experiment.
Built to save time, reduce errors, and standardize validation—so you can move science forward with confidence and precision.
Trusted by the world’s top labs.
What is a Protocol?
Think of it as a scientific recipe. But unlike a static recipe,
Customized Protocols
Each protocol’s workflow is tailored to fit your experiment’s specific needs, ranging from calculations to downstream preparation.
How-To Videos
Every protocol includes step-by-step video demonstrations, ensuring techniques are clearly shown, not just described.
Quality Management
Proactively monitor Quality Assurance (QA), Quality Control (QC), and Quality Improvement (QI) to mitigate risk.
Seamless Integration
Compatible with LIMS, ELNs, and laboratory infrastructure.
Fully Scalable
Designed to work for a single bench or across global research networks.
Future Proof
Protocol-Plus automatically stays up to date with regulatory bodies.
Get Started in Minutes
Whether you’re writing your first protocol or scaling across clinical networks, Protocol-Plus makes it simple.
Why Choose Us
Metrics That Move The Needle
90%
Reproducibility
Across Users
95%
Compliance Alignment
85%
Improved
COGS
Tiered Pricing for Scalability
Starter
For small labs or early-stage researchers.
Professional
For growing labs ready to scale with reproducibility and compliance.
Enterprise
For institutions and CROs with advanced workflows and multi-lab teams.
Platform Features
Continuity, Compliance, & Reliability
Testimonials
Value Beyond the Laboratory
Protocol-Plus gives technicians clear instructions, helps managers run operations efficiently, allows leaders to remain audit-ready, and builds scientists’ confidence in delivering reliable and compliant results.
Whether preparing for funding, working with regulators, or achieving outcomes that benefit patients, Protocol-Plus supports every stakeholder in moving forward with trust and accuracy.
Technician Empowerment
“I’m still early in my training, but with Protocol-Plus, I don’t feel lost. The guided steps, videos, and clear logic let me do the work confidently and consistently.”
Laboratory Technician, Oncology Research Lab
Operational
Efficiency
“I’m still early in my training, but with Protocol-Plus, I don’t feel lost. The guided steps, videos, and clear logic let me do the work confidently and consistently.”
Laboratory Technician, Oncology Research Lab
Audit
Confidence
“We stay inspection-ready by default. Our team can focus on science, not scrambling for paperwork. The technicians are happy and so is leadership.”
Laboratory Technician, Oncology Research Lab
FDA Regulatory Reviewer
“The clarity and completeness of the Protocol-Plus documentation significantly accelerated our review process. Each protocol was logically structured, evidence-backed, and fully aligned with FDA expectations. It minimized back-and-forth, reduced ambiguity, and demonstrated a level of preparation we rarely see—especially from early-stage teams.”
CAP/CLIA Lab Inspector
“Protocol-Plus made this one of the most straightforward inspections I’ve conducted in years. Every requirement—from procedural traceability to calculation logic—was fulfilled with clarity and consistency. The protocols were not only compliant but structured in a way that made review seamless. This level of transparency and standardization should be the norm across regulated labs.”
Protocol-Plus in Action: Real-World Case Studies
Explore how leading research teams are using Protocol-Plus to overcome challenges in reproducibility, compliance, and global scale-up—faster and with greater confidence.
Biomarker Reproducibility
Multi-lab validation of oncology biomarkers across 4 partners. Protocol-Plus helped improve reproducibility to 93% and reduced validation cycle time by 4.5 months.
- 93% reproducibility
- CLIA & CAP compliant
- 4.5 months saved
Diagnostics Submission Readiness
A startup preparing for FDA 510(k) used Protocol-Plus to align protocols and resolve 14 inconsistencies before submission.
- 100% audit traceability
- 6 months saved
- Embedded training videos
Global Research Scale-Up
A cell therapy program across the US, Germany, and Singapore standardized pre-clinical workflows using Protocol-Plus to reduce deviations by 70%.
- Cross-region SOP alignment
- 70% fewer deviations
- Live updates across 12 teams
Meet Protocol-Plus
From the front lines of scientific innovation to your laboratory bench
Our team has decades of experience in translational medicine, diagnostics, regulatory strategy, and quality systems. We’ve authored protocols, led compliance audits, and driven innovations that transformed patient care. This expertise is now integrated into every aspect of Protocol-Plus.