Empower your CRAs Strengthen your clinical operations.

Menken Monitor is the first workspace designed specifically for Clinical Research Associates, helping them stay organized, compliant, and efficient across every study and site.

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CRAs need better tools

CRAs are responsible for site performance, protocol compliance, data quality, ultimately impacting patient safety. But their daily workflows are spread across disconnected systems: spreadsheets, calendars, trackers, email, and local files.

The result?


No more missed deadlines

What Menken Monitor brings to your organization

Consistent Monitoring Quality Across Trials

Menken Monitor centralizes CRA activity, documentation status, visit outcomes, and overdue items into a single source of truth. Line managers and study leaders have a clearer visibility into site performance, reporting timelines, and compliance risks, reducing findings and improving inspection readiness across studies.

Increased Efficiency & Reduced Administrative Load

Automations reduce repetitive admin tasks like calculating monitoring visit windows, tracking deadlines, chasing reports, and managing follow-ups. CRAs spend less time navigating trackers and emails, and more time focusing on quality monitoring, patient safety, and timely issue resolution.

Standardized Onboarding That Accelerates CRA Readiness

Built-in checklists, visit guides, templates, and structured workflows help new CRAs get up to speed faster and with fewer mistakes. Menken Monitor standardizes expectations and provides step-by-step support, enabling teams to scale efficiently while maintaining consistent monitoring quality.

Menken Monitor solves this

It consolidates everything into a single, intuitive workspace, built with CRAs, for CRAs.

Never Lose Oversight or Data Again

When CRAs leave, companies lose continuity, context, and institutional memory.
MenkenMonitor stops that bleed: every note, checklist, deviation, and risk signal stays with company, not the individual.

Turnover stops being a threat to study quality.

Standardised Guidance for Every Study

Monitoring quality should not depend on who is assigned.

MenkenMonitor enforces company-wide monitoring standards, checklists, and mandatory workflows.

No more forgotten tasks, inconsistent documentation, or ad-hoc work habits.

Monitoring Schedule That Never Slips

Late visits = findings, delays, escalations.

MenkenMonitor tracks visit windows, overdue tasks, expected timelines — and alerts your team before risk materialises.

Your oversight becomes proactive, not reactive.

Real-Time Visibility Into Study Health (no waiting for reports)

Companies currently wait weeks for monitoring reports and rely on handwritten notes or inconsistent visit summaries. MenkenMonitor gives you live dashboards:


  • open issues
  • pending actions
  • protocol deviations
  • missing data
  • site performance

You see problems the moment they appear — not four visits later.

Enforced Quality & Compliance Across All CRAs

You cannot rely on every CRA having the same experience, discipline, or attention to detail. MenkenMonitor enforces compliance:

  • required fields
  • required evidence
  • deviation logging
  • visit preparation steps
  • reporting templates

This removes variability and protects the company from audit findings caused by human inconsistency.

I work on 4 protocols at the same time across 10 sites — my calendar is always packed. Having a single view to track everything in one place is a game-changer!

Venkatesh Prasanna
CRA

Empower CRAs with Menken Monitor. Empower your CRAs with better oversight, automation, and structured workflows that reduce administrative load, strengthen compliance, and keep every monitoring activity on track.

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