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HomeConnected systemsCLINICAL RESEARCH REPORTING
CLINICAL RESEARCH REPORTING

See study progress across the systems behind it.

Connect clinical operations reporting across Veeva EDC, Clinical Operations, CTMS, eTMF and Study Startup, subject to your licensed interfaces and approved data scope.

Discuss your reportingSee a related workflow
Prepared around your sources, definitions and users. We agree access, setup, delivery scope and pricing before an assisted trial.
CLINICAL OPERATIONS

Make the reporting useful across your business.

Study teams can spend too much time assembling updates from separate systems. A defined reporting layer can bring milestones, site activation, document status and selected EDC operational measures into a consistent view for study and portfolio reviews.

How we prepare business context

Questions the reporting can help you explore

  • Which sites are waiting on a study startup milestone?
  • Where do document completeness and operational status differ?
  • Which studies or sites need attention in the next review?
AGREE THE REPORTING FOUNDATION

The right data, with the right definitions.

Potential sources in your scope

  • Veeva Clinical Operations, CTMS and study metadata
  • Study Startup milestones and site activation information
  • eTMF document metadata and approved completeness measures
  • Permitted EDC operational status or approved extracts

Your rules and reporting context

Agree study and site identifiers, milestone definitions, expected documents and reporting cutoffs. Keep the source and refresh time visible so users understand what an operational measure represents.

What we check during preparation

Access differs across Veeva products and customer configurations. Confirm the approved API or export method, licensed access, roles, hosting region and data minimisation. Validation requirements are agreed with your governance team. The reporting layer supports operational oversight and does not replace the source clinical systems or their controls.

HOSTING AND DELIVERY

A reporting service your team can work with.

DataNova can manage the analytics environment, data pipelines and reporting as part of an agreed delivery scope. Choose a scoped implementation or ongoing Managed BI, which includes the platform subscription.

  1. 01

    Scope the connection

    Confirm the systems, permitted interfaces, data volume, reporting questions and refresh expectations.

  2. 02

    Prepare and reconcile

    Map the data into Fabric, apply the agreed definitions and compare reporting totals with the source.

  3. 03

    Run and improve

    Agree hosting, access, monitoring and support responsibilities. Review the reports with the people using them.

Explore Managed BI and ongoing support

Source-system licences, tenant access and any additional integration costs are confirmed in the quote. Hosting location and responsibilities are agreed for your organisation.

A RELATED DATANOVA WORKFLOW

Proactive email insights

Bring a focused data briefing into the working day.

This demonstration uses example data to show a related DataNova workflow. Your source connection and reporting setup are prepared separately.

Open the video and transcript
Read the transcript

The AI-assisted briefing brings the findings into plain language: what is positive, what needs attention, what actions to consider, and what to monitor next. The briefing can reach the person who needs it by email. The email presents the important findings in a readable form, with a route back into the application. For clients, this can become a morning briefing about the previous twenty-four hours, a weekly review of the important movements, or an alert when an agreed condition is met: margin pressure, spending beyond tolerance, or a forecast stock shortfall. This is proactive intelligence: bringing a focused, evidence-backed update to the people who need to make a decision.

START WITH YOUR PROCESS

Let's discuss Clinical research reporting.

Share your requirements. No card or commitment.

Describe the result you need and the information you work with. We can help you identify a suitable existing application or scope a tailored pilot.

  1. Share the problem and your data sources.
  2. Discuss the workflow and a practical starting point.
  3. Agree the scope, costs and trial route.
No card is needed to make an enquiry.

A card is required when you start a trial. An enquiry does not start a subscription or commit you to a project.

Where is your data today? Optional, choose any
What should the application help with? Optional, choose any

We use these details to respond to your enquiry. Read our privacy policy. Please describe the systems you use without including passwords or customer records.

EVALUATE THE RIGHT FIT

Try the application before committing to the next step.

Both assisted routes include a 30 day free trial, starting after onboarding and environment setup. Card required at signup. No charge until your 30 day trial ends.

Existing app that fits

Start without an implementation fee.

If an existing application meets your requirements without additional mapping or implementation, implementation and the 30 day trial are free. Normal subscription charges begin after the trial, under your agreed terms.

Mapping or custom work needed

Agree the full quote before the pilot.

We agree the application, mapping, workflows and implementation quote upfront. We then prepare the agreed pilot for your 30 day free trial. If you choose to proceed afterwards, the quoted implementation fee and monthly subscription become payable.

We confirm the pilot deliverables, preparation, trial start and decision process together. Any work beyond the agreed pilot scope is discussed separately.

USEFUL ANSWERS

Before we connect your data.

Can EDC, CTMS, eTMF and Study Startup use one reporting view?+

They can be brought into a scoped reporting model where permitted interfaces and consistent study or site identifiers are available. We confirm the data that can be accessed, how measures are defined and the controls needed before preparing a pilot. We do not assume patient-level data is required for operational reporting.

Can DataNova handle hosting and ongoing reporting?+

Yes. We can include analytics hosting, pipelines, reporting and ongoing support in an agreed Managed BI scope. The platform subscription is included in Managed BI. The included plan, source licences, preparation and service responsibilities are confirmed before you commit.

When does the assisted trial begin?+

Your 30 day assisted trial begins after onboarding and environment setup. A card is required at signup. You are not charged until your 30 day trial ends. Where mapping or custom work is needed, the implementation quote and pilot scope are agreed upfront. The quoted implementation and monthly fees become payable if you choose to proceed after the trial.

GO BEYOND THE REPORT

Connect the insight to a business workflow.

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