More validation capacityfor the team you have.

A team of two or three owns the LIMS, the QMS, the ERP, and every upgrade to them. Merivane takes the scripting, the execution, and the documentation off their desk. Your team keeps the review, the takeover, and the signature.

The whole chain, on the systems you already run.
  1. Approved requirement
  2. Test scripts
  3. Autonomous execution
  4. You take over
  5. Defects logged
  6. Signed OQ / PQ report
The situation

Three people. Seven systems. One audit calendar.

The validation backlog blocks upgrades. Consultants cost per protocol. Evidence sits in shared drives, hard to find when an auditor asks.

  • The backlog blocks upgradesA vendor release waits until the team has time to validate it.
  • Consultants cost per protocolEvery OQ or PQ is a new engagement.
  • Evidence sits in shared drivesScreenshots and spreadsheets, hard to trace back to a step.
Validation backlog3 items
LIMS upgradeBlocked, 6 weeks
QMS periodic reviewDue
ERP patchWaiting on consultant
What changes

The same validation. Days, not months.

Merivane drafts the scripts, runs them, captures the evidence, builds the RTM, and drafts the report. Your team checks each output, corrects it where needed, and signs.

  • The repetitive work moves to MerivaneScripting, clicking through steps, and filing screenshots.
  • Your team spends its time on reviewEvery output is checked and signed by a person.
  • Evidence is captured, not filedNo shared drive to search through later.
Your team's timeOne OQ, one system
TodayWith Merivane
Write scriptsWeeksHours, to review
ExecuteWeeksHours, on call
Capture evidenceHoursAutomatic
Build RTMWeeksAutomatic
Write reportWeeksHours, to review
Review and signHoursSame
Control

Your QA stays the approver of record.

Nothing executes before your team approves the scripts. Your team can take over any step, and compliance determination stays with you.

  • Nothing executes before approvalScripts run only after your QA locks them.
  • Take over any stepScreens change. Your team steps in, then hands control back.
  • Compliance determination stays with youMerivane supplies the controls and the evidence.
Step 4 needs youExpected the approval confirmation. Seen: a session time-out warning. Take over, or skip this step and continue.
Take overSkip step
Priya N. completed step 42 screenshots captured · returned control at 14:33:10 UTC
Getting started

Start with one system and one requirement.

A short pilot on a UAT system shows the whole chain before you commit to more.

Now onboarding validation pilot partners
Getting started3 steps
1
Pilot

One approved requirement, one UAT system, 45 minutes.

2
First OQ

Run the first OQ on the UAT system.

3
Schedule

Upgrades and periodic review on a schedule.

A typical stack

Any browser-based GxP system you can give a test account to.

LIMSQMSERPeDMSTraining LMSMES

Questions about small and mid-sized pharma.

If your question is not here, ask us. We reply within one working day.

Does IT need to install anything?

No. Merivane works on the browser UI with a test account.

How long is onboarding?

One pilot session, then the first OQ in the first weeks.

Can our consultant work in it with us?

Yes, with a role you set.

What does our team still do?

Approve the scripts, take over when a screen changes, review the defects, and sign the report. Merivane does the scripting, the execution, and the documentation in between.

What do we need to have ready?

One approved requirement document and a test account on a UAT system.

Now onboarding validation pilot partners

See a full run on one of your systems.

Bring one approved requirement. We show you the chain end to end, on a system you already use, in under an hour.

Book a demo
Reply timeOne working day
FormatLive run, 45 minutes