01
Learn
Understand epigenetics and biological aging.
Education comes before any commercial consideration.
The Test
Make the science understandable
What the assessment is, why it matters, how it works, what you will learn, and what it cannot tell you.
What is it?
A concise clinical definition of the epigenetic assessment.
Why does it matter?
Explain biological aging and why chronological age is incomplete.
How does it work?
Sample → DNA → methylation analysis → validated model → report.
What will I learn?
Show report modules without promising unsupported outcomes.
What can it not tell me?
Explicit limitations, non-diagnostic boundaries and uncertainty.
01 — What is it?
A concise clinical definition of the epigenetic assessment.
VERITAS EPIGENETIC is an advanced epigenetic assessment designed to analyse DNA methylation patterns associated with biological aging and selected health-related pathways.
It studies epigenetic marks. It does not modify DNA. It is not a diagnostic test for any disease, and it does not estimate lifespan.
The output is a structured biological-aging profile delivered with methodology, references, evidence level and limitations.
02 — Why does it matter?
Explain biological aging and why chronological age is incomplete.
Your chronological age tells one story. Your biology tells another.
Chronological age is a simple number: time since birth. Epigenetic information is made of DNA methylation patterns and validated molecular measurements, placed in appropriate clinical context.
03 — How does it work?
Sample → DNA → methylation analysis → validated model → report.
The user journey should never feel like “buy kit → receive score”. It should feel like a medical information pathway.
02
Consult
Determine whether testing is appropriate.
Indications, intended use, target population and appropriate clinical context.
03
Test
Collect the validated biological sample.
Ordering workflow, sample requirements, logistics and turnaround information.
04
Analyze
Laboratory processing + quality control + computational analysis.
Sample processing → DNA extraction → methylation analysis → quality control → computational analysis.
05
Understand
Receive a structured biological-aging report.
Explain result + evidence + limitations + questions for physician.
06
Discuss
Review findings with a qualified healthcare professional.
Turn the report into a clinical conversation.
04 — What will I learn?
Your Biological Aging Profile
A structured view of validated epigenetic measures. Show report modules without promising unsupported outcomes.
Executive summary
High-level interpretation in plain clinical language.
Every module carries its evidence level, reference information and limitations.
Executive summaryModule
Epigenetic ageModule
Age accelerationModule
Biological aging domainsModule
Metabolic contextModule
What this does / does not meanModule
05 — What can it not tell me?
Explicit limitations, non-diagnostic boundaries and uncertainty.
Make limitations visible. A transparent limitation is a trust signal.
It does not predict lifespan
No life expectancy, no countdown, no individual longevity forecast.
It does not diagnose disease
The assessment is not a diagnostic test and does not replace clinical investigation.
It does not establish causation
Associations described in the literature do not explain an individual result.
It does not reverse aging
We make no claims about reversing, turning back or stopping biological aging.
It does not stand alone
Results require interpretation by a qualified healthcare professional.
It carries uncertainty
Every measure is reported with its confidence and reference limitations.
Measure
Validated laboratory methodology under a documented quality system.
Interpret
Structured analysis using validated computational models.
Contextualise
Placed alongside clinical history and conventional investigations.
Educate
Explained in plain clinical language, with references.
Common questions
About the assessment
Blood, saliva or another validated sample. The final specimen type is confirmed with the validated assay and published in the sample requirements for ordering clinicians.
Turnaround information is published with the ordering workflow once laboratory operations are finalised. Laboratory information to be added.
The platform is designed around medical oversight. Requirements depend on the regulatory framework in your jurisdiction; regulatory documentation to be provided.
Data access options are described in the consent and data-protection documentation on the Quality, Regulatory & Privacy page.
What this does not mean
Content on this page describes the intended design of the assessment. Domains, performance characteristics and regulatory statements are published only once verified by the responsible medical, scientific and legal teams.