Lambros Analytics

Our Services

Specialized support across the drug lifecycle

Lambros provides biostatistical consulting and statistical programming services tailored to your study needs, timelines, and regulatory expectations — with SOP-driven quality and documentation.

Biostatistics SAS Programming CDISC SDTM / ADaM TLFs BA/BE & PK/PD IVRT / IVPT
Clinical statistics and programming support

Delivery

Regulatory-ready outputs

Quality

SOP-based QC workflow

Standards

CDISC aligned delivery

What we do

Services built for speed, accuracy, and compliance

From analysis planning to submission packages, we support your teams with consistent execution, transparent communication, and documentation-ready outputs.

Core

Biostatistics & Statistical Programming

End-to-end programming and analysis support — from planning to regulatory-ready outputs.

  • SAP support & analysis
  • TLFs and CSR support
  • Integrated analyses (ISS/ISE)
  • Submission package readiness
SAS QC Documentation

Standards

CDISC SDTM / ADaM Implementation

Standardization aligned to CDISC models with traceability and validation readiness.

  • SDTM / ADaM conversion
  • define.xml support
  • Reviewer’s guides
  • Validation & QC support
SDTM ADaM Pinnacle21

Outputs

Tables, Listings & Figures (TLFs)

High-quality TLF generation and QC workflows supporting clinical and regulatory reporting.

  • Output shells & programming
  • Consistency checks
  • CSR-ready formatting
  • Review cycle support
CSR Shells QC Cycles

Focus

SOP-led

Quality checks and documentation driven delivery.

Speed

FSP-ready

Flexible resourcing with predictable output cycles.

Compliance

CDISC

Traceable SDTM/ADaM workflows & validation.

Outcomes

TLFs

CSR-ready tables, listings, and figures.

Studies

BA/BE & PK/PD statistical support

Statistical analysis and reporting support for BA/BE and PK/PD studies with strong documentation, clear traceability, and review-friendly outputs.

Analysis support

PK parameter summaries and comparative statistics.

Reporting outputs

Report-ready tables and figures with QC.

BA/BE and PK/PD support
In-vitro statistical services

In-Vitro

IVRT / IVPT and dissolution analytics

In-vitro analytics and statistical comparisons supporting formulation and performance evaluation. Clear outputs designed for review and decision-making.

  • • IVRT / IVPT analysis
  • • Dissolution profile comparisons
  • • Stability trend analytics
  • • Clear reporting outputs

How we work

A simple engagement flow

Clear scope, strong execution, and consistent communication from start to delivery.

Step 01

Requirement

We align on scope, timelines, standards and review expectations.

Scope Timelines Standards
Step 02

Plan

We share milestones, roles, risks and deliverable structure.

Milestones Roles Risks
Step 03

Execute

Programming and analysis with SOP-based checks and tracking.

SOP QC Tracking
Step 04

Deliver

Final outputs with documentation and review cycle support.

Outputs Docs Review

Ready to discuss your requirement?

Share your scope and timelines — we’ll respond with a structured approach.