Valexios

AI-POWERED VALIDATION FOR LIFE SCIENCES

THE VALEXIOS PLATFORM · IN DEVELOPMENT

Validation.
Connected.
With clarity.

Connect what you know, the work you do and the evidence behind every decision. A validation platform being built for life sciences teams—from first plans to ongoing assurance.

A connected workspace for validation, from plan to periodic review.

PLANNED PRODUCT EXPERIENCEILLUSTRATIVE DATA
VValexios / Programme overviewVL

SITE VALIDATION PROGRAMME

The whole lifecycle, in view.

Design preview
Validation basis07 / 09

Approved records

Periodic reviews03

Require attention

EQUIPMENT & SYSTEMS VALIDATION BASIS
⌘ Purified water systemUtilities · PW-001Approved
⌘ Manufacturing vesselEquipment · MV-002Approved
⌘ Cleaning processProcess · CLN-001Under review
↗
Validation master planConnected to scope, ownership and evidence
↗
✓
See the status. Follow the evidence.

From programme oversight to the individual record.

DESIGNED FOR

Validation engineers

+

Quality teams

+

Programme leaders

THE PLATFORM

01 / CONNECT

The whole picture.
Down to the evidence.

Validation is more than a collection of documents. Valexios is being designed to connect the programme, the individual asset, and the evidence behind its status.

VALEXIOS / PRODUCT DESIGN PREVIEW
Valexios design prototype showing programme oversight and validation master plan visibility
One programme. A shared view.

Bring the validation master plan, active work, ownership and upcoming reviews into the same conversation.

Concept interface · Illustrative data

WHEREVER YOUR TEAM STARTS

YOUR KNOWLEDGE. YOUR NEXT STEP.

A connected future.
Your starting point.

Building your first validation framework, moving beyond paper, or working alongside an eQMS? We’re designing Valexios around the knowledge and controls your team already has.

START WITH A CLEAR FOUNDATION

Make the first steps
the right steps.

Bring intended use, responsibilities and the validation approach into focus before formal execution. The planned setup journey helps teams identify the controls and knowledge they need to establish.

Discuss your starting point ↗
PLANNED JOURNEY
  1. 01Define the intended use
  2. 02Establish the governing controls
  3. 03Prepare, review and execute

Templates support preparation. Your authorised team adopts the procedures and makes the decisions.

Onboarding and integration capabilities are in design. Contact us to discuss fit and availability.

CONNECTED FROM START TO REVIEW

02 / FOLLOW THROUGH

Validation doesn’t end
at approval.

Keep the thread intact as equipment, systems and processes move from initial qualification into everyday operation and ongoing review.

START WITH THE VALIDATION BASIS

Give every activity a reason.

Establish scope, responsibilities and the validation strategy. Connect your validation master plan to the equipment, systems and processes it governs.

Validation master plan↓Asset & process register↓Defined scope & ownership

A CLEARER VIEW OF READINESS

Progress is one signal.
Readiness needs context.

01 /

Validation basis

Understand the approved scope and evidence supporting an equipment, system or process validation state.

02 /

Operational release

See the release decision and any conditions that need attention before use.

03 /

Ongoing assurance

Keep periodic reviews, changes and open actions visible beyond the project’s completion.

AI VALIDATION COACH

A thinking partner.
Right where
you work.

Ask about a task, work through a validation question, or prepare a first draft. Our planned AI Coach brings guidance closer to the work, with sources and context you can inspect.

Discuss your use case ↗

Planned capability. Current prototype uses sample responses.

✳Validation CoachCONCEPT

What should I check before starting a periodic review?

ILLUSTRATIVE GUIDANCE

Review the applicable procedure, previous conclusions and the records covering the review period.

  • What has changed since the last review?
  • Which events or actions remain unresolved?
  • What evidence supports the proposed conclusion?
Designed to show the basis
Document, revision and supporting passage—so you can inspect the context before using a suggestion.
Guidance and drafts remain subject to qualified human review.

HOW AI SHOULD HELP

From knowledge
to a better first draft.

Our planned AI experience connects guidance to the task and its sources. Engineering judgement and quality decisions stay with your team.

01 / UNDERSTAND

Find the context.

Bring together the relevant requirements, procedures and reviewed records for the work at hand.

02 / PREPARE

Make the work clearer.

Propose requirements, test outlines and review questions. Expose assumptions and missing information.

03 / REVIEW

Keep people in control.

Inspect sources, edit suggestions and route accepted drafts through the defined review process.

✳

AI helps explain and prepare. It does not create original test evidence, authorise release or replace a quality decision.

OUR APPROACH

Built around the work.
Shaped with the people.

Valexios is an emerging software platform for life sciences validation. We are starting with equipment qualification and designing for a connected lifecycle across teams and records.

Our direction is simple: make the validation basis easier to understand, the evidence easier to follow, and the next action easier to see.

We’re inviting validation engineers, quality professionals and programme leaders to help shape that experience.

Join the conversation ↗

THE PEOPLE BEHIND VALEXIOS

A shared ambition.
A clearer way forward.

Founded by Ahmed Hassan and Mohamed ElSayed to shape a more connected approach to validation.

CO-FOUNDER · ORIGINAL IDEA

Ahmed Hassan

Ahmed originated the idea for Valexios: bringing validation knowledge, workflows and evidence together in one connected platform.

CO-FOUNDER · INFRASTRUCTURE

Mohamed ElSayed

Mohamed leads the infrastructure work, establishing the cloud foundation that will support the Valexios platform.

A FEW THINGS TO KNOW

Good questions.
Clear answers.

Is Valexios available today?

Valexios is in development. The interfaces shown here are design prototypes with illustrative data. Contact us to discuss your workflow, see the concept and explore future early-access opportunities.

What is the initial focus?

We are starting with equipment qualification: planning, requirements, risk, protocols, execution, evidence and review. The wider design connects programme oversight and ongoing assurance.

Will the AI Coach make approval decisions?

The planned Coach supports questions, explanations and draft preparation. Approval and release decisions remain with authorised people through the defined quality workflow.

Does Valexios replace our QMS?

Our focus is the validation lifecycle. For teams with an existing QMS, we are designing clear boundaries between validation records and the procedures, deviations or training records owned elsewhere. Specific integrations are not yet available.

Can we bring existing paper records?

We are designing a reviewed adoption journey for existing knowledge. Imported records would need checks for completeness, provenance and applicability; importing a file would not automatically establish an approved validation state.

Can we discuss our team’s requirements?

Yes. We would like to understand how your team plans work, manages evidence, assesses status and performs periodic reviews. Email info@valexios.com to begin the conversation.

START A CONVERSATION

Better validation starts
with your experience.

Show us how your team works today.
Help shape what validation can look like tomorrow.

Email the Valexios team

Opens your email app

Valexios product design preview

Concept interface · Illustrative data · Product in development