Print on Demand for Clinical Trial Documentation

Your reliable partner for clinical trial printing

Mimeo supports pharmaceutical companies and CROs with the printing and distribution of sensitive trial documents — with consistent quality and reliable delivery, from a single site to a global study.
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Print on Demand

Is every site on the same version?

Protocol amendments shouldn't leave outdated materials in circulation.

Always current, always compliant

Update documents any time and ensure only the current, approved version is in circulation.

Consistent across every site

All materials are produced to the same specifications regardless of location, ensuring consistent quality across every trial site.

Built for sensitive study documents

Reliable print quality for regulatory-relevant materials (e.g. CRFs, ISF binders) processed with the precision daily trial operations demand.

Get Started with Print for Your Next Study

See how much coordination time your clinical team can get back.

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Clinical Operations Support

Too many sites to coordinate?

Centralise print and distribution so study teams focus on the trial, not logistics.

Less coordination, more control

Central management of print and distribution reduces coordination with multiple suppliers, relieving clinical and study teams significantly.

Structured for recurring studies

Standardise the creation and ordering of documents for recurring study workflows — improving efficiency and minimising errors.

Worldwide delivery, fully tracked

Ship study documents reliably to investigator sites worldwide, with shipment tracking and predictable delivery times.
Clinical trial printing

Mimeo's Platforms

What Mimeo Can Do for You

Mimeo helps pharmaceutical companies and clinical teams manage, produce, and distribute trial documents efficiently, compliantly, and reliably. Our digital solutions reduce manual effort and ensure teams always work with the latest approved versions.

Mimeo Print

Upload trial documents, configure ISF binders or CRFs, and release for printing exactly when they're needed — always in the current version.
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Mimeo Digital

Distribute trial documents digitally and securely, for rapid access by internal teams and investigator sites.
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Mimeo Marketplace

A central platform for all approved trial documents — investigator sites and teams worldwide can access or order independently, with full version control.
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Integrate A Branded Storefront: Mimeo Marketplace

Empower your audience with the ability to order what they need when they want. Publish your on demand print, digital or warehoused items to a custom storefront.

clinical trial ringbinder

Clinical Trial Materials – Simple, Secure, Efficient

Clinical Trial Materials, Done Right

A secure, cost-effective way to print and distribute your trial documents.

Regulatory Binders & ISF Folders

Structured filing and secure organisation of central trial documents.

Study Reference Manuals

Clear, easy-to-understand reference materials for study and site teams.

Case Report Forms (CRF)

Precise, structured printing for consistent data collection.
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Mimeo Digital: The First Courseware Distribution Platform

Empower your learners, encourage collaboration, and deliver content in any format, to any device, anywhere in the world. You keep control of the content while providing your end-users an easy, high-end virtual content experience.

Integrations

Seamlessly Print, Manage, and Distribute from Your Own Systems

Mimeo APIs

Take advantage of Mimeo’s secure APIs and connect your existing IT infrastructures for seamless document print and distribution control.
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See Our Print Quality for Yourself!

Request a free sample of your clinical trial binders and check paper quality, print, and binding before making your decision.

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Frequently Asked Questions

Here are some of our most frequently asked questions about our business services and platforms.

Clinical trial documents include all materials required for the planning, conduct, and documentation of clinical studies – e.g. Investigator Brochures, ISF Binders, patient diaries, or training manuals.

Many clinical trials are subject to regulatory requirements for registration or publication (e.g. ClinicalTrials.gov or the ISRCTN registry). The specific requirements depend on study design and region.

Yes. Mimeo supports international production and distribution from our UK, US, and European facilities.

With Print on Demand, new versions can be uploaded and produced immediately, ensuring only the current, approved version reaches study sites.

Yes – especially for organisations with recurring needs across multiple sites and studies.

Including CRFs, patient materials, forms, manuals, study kits, and documentation sets.

No – print flexibly on demand, from a single copy upwards.

Still Have Questions?

Contact our support team for further assistance

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