Achievements
Delivery you can trust — built step-by-step
A snapshot of capability, consistency, and quality — built through SOP-driven execution, secured workflows, and regulatory-ready outputs.
SOP-led execution
Structured review + traceability.
Secure delivery
Confidential & controlled workflows.
Highlights
Quality • Timelines • Trust
Clients
CDISC
In-Vitro
Consistent outputs with structured QC checkpoints and clear delivery tracking.
Healthcare Domain Clients
CDISC Standardizations
In-Vitro Projects Delivered
Clinical Domains Supported
Operational strengths
Disciplined execution matters most in regulated environments. Our process is built to reduce review cycles and rework.
Established SOPs
Documented checks across domains.
Quality policy
Review workflows & traceability.
Licensed tools
Reporting stack aligned to standards.
Secured delivery
Secure connectivity practices.
Quality Snapshot
SOP • QC • DeliveryWe prioritize reproducibility to reduce rework and improve review confidence.
Growth Timeline
Achievements — year by year
A clear view of how Lambros evolved from foundation to consistent delivery.
2021
FoundationProcesses & SOP-first delivery
- Built SOPs and QC checkpoints for delivery
- Established secure delivery practices and documentation
2022
StandardizationCDISC workflows matured
- Expanded SDTM/ADaM standardization delivery
- Improved traceability and review-ready outputs
2023
ExpansionBroader analytics + delivery capacity
- Expanded support for In-vitro and BA/BE statistics
- Scaled clinical domain coverage with stable QC processes
2024–Present
TodayConsistent delivery at scale
- Repeatable delivery model with reliable timelines
- Growing partnerships and healthcare client base
What this means for clients
You get a stable delivery partner with SOP discipline, QC rigor, and outputs designed to reduce review cycles.
Clear execution model
Scope → Plan → Execute → Deliver
Quality-first workflows
SOP + QC checkpoints
Trusted outputs
Regulatory-ready reporting
Capabilities
Expertise areas
Support across biostatistical analysis, programming, and standards.
Equivalence / Non-inferiority
Analysis strategies for comparative studies with appropriate reporting.
Mixed Models & Repeated Measures
Robust models, multiple comparisons, and clean interpretation outputs.
Survival & Categorical Data
Time-to-event and categorical analysis with regulatory-ready summaries.
Dose Proportionality
Steady state and dose proportionality analysis for PK studies.
CDISC Standardization
Efficient SDTM/ADaM workflows and integrated deliverables.
QC & Review Support
Documentation, traceability, and structured review cycle support.
Want to validate scope and timelines?
Share your requirement — we’ll respond with a structured plan and delivery approach.