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Who We Help

Pubrica supports eight groups of clients: researchers and authors, students, physicians, universities, pharma and biotech companies, medical device manufacturers, publishers, and education and assessment providers. Every group has access to the same catalogue of editing, writing, statistics, regulatory and publication services. What differs is the standard the work must meet, who reads the finished document, and whether the price is published or quoted. Choose the page that describes you to see the services most relevant to your work.

  • Two pricing models: published prices for individual authors, and scoped quotations for organisations
  • The same experts for every client — work is assigned by subject rather than by account size
  • A free first step for every service, carried out on your own document before you commit
  • Work built to your required standard, whether that standard is set by a journal, a regulator, a notified body, a payer or an awarding body
  • If no audience page fits, use the service menu, which is organised by type of work and offers the same services
Pricing by audience Pricing model

Researchers, students, cliniciansPublished prices

InstitutionsRetained or per project

Pharma, biotech, deviceQuoted per programme

Publishers and societiesPer article or retained

Education and assessmentQuoted per programme

Your audience → your required standard → the work → the standard met

For every audience
  • Assigned by subject, not by account size
  • A free first step on your own document
  • Current version of each standard stated
  • Working files handed over
  • Service limits stated in advance
Eight audience pagesOne service catalogue
From $0.025 a wordWhere prices are published
Quoted per programmeWhere they are not
ISO 9001:2015Quality management certified · cert. H3CR9TCU20251212INDQM10N

Our Services

Services for Each Audience

The audiences fall into two groups: authors publishing their own work, and organisations whose work is assessed by a regulator, notified body, payer or awarding body.

Researchers & authors · prices printed Subject-specialist editing, biostatistics, and submission support through to reviewer responses. The reporting-guideline check is free.

Publishing your own workMost desk rejections result from an unmet reporting guideline or a claim the data does not support, rather than from the English.

Students & early career · from $0.025 a word Thesis and dissertation editing within the IPEd guidelines, with structural issues described for the student to resolve, and support with a first journal submission.

Editing limits for thesesExaminers assume the argument is the student’s own. We identify weak arguments and leave the revision to the student.

Physicians & clinicians · quoted Case reports written to CARE with patient consent documented first, clinical literature reviews, original research from your own case series, and CME content, prepared around clinical schedules.

Working around clinical timeWe work from notes, a dictation or a twenty-minute call, so a finished draft is not required.

Universities & institutions · retained or per project Additional capacity for core facilities: statistics, database builds in your own instance, funder data management plans, and researcher training.

Working to your standardsMost cores are limited by capacity rather than willingness. Work built to their conventions can be supported by the core afterwards.

Pharma & biotech · quoted per programme Regulatory writing, medical communications, market access and biometrics built from one evidence core, written to the current version of each standard, which we name in the document.

Consistency across documentsWhen documents are split across suppliers, the same endpoint can be described in different ways, and assessors notice the inconsistency.

Medical device & IVD · quoted per device Technical documentation for notified body assessment under MDR and IVDR: evaluation plans and reports, PMCF, PMS and PSUR by class, SSCP, risk file and GSPR checklist.

Device-specific regulationTreating device regulation as a variant of pharma regulation causes most of the deficiencies notified bodies raise.

Journals, publishers & societies · per article or retained Editorial operations in your own submission system, integrity cases handled to COPE flowcharts, statistical and search-strategy review, and evidenced accessibility conformance.

Editorial decisions stay with youYour editors make all editorial decisions. We provide capacity and do not take over the running of the journal.

Education & assessment providers · quoted per programme Curriculum and standards mapping evidenced item by item, item writing and review, six psychometric services sold separately, bias and fairness review, and delivery to your platform.

Psychometric services sold separatelyMost providers need two of the six psychometric services in a year, so each service can be purchased on its own.

Samples are illustrative and anonymised. Hover any one of them to play it again.

Compliance and Standards

Standards We Apply Across All Audiences

Each audience answers to different standards, and for every one we work to the version currently in force.

ICMJE and COPE (for anything going to a journal)

Authorship criteria, declarations, and the rule that editing and writing support is acknowledged rather than credited as authorship.

E6(R3)

ICH, MDR and IVDR (for anything going to a regulator)

We work to the version in force rather than the version a template was built on, and we name the version used in the document.

2.2 / 508

Accessibility (for anything published digitally)

Conformance is evidenced with a report rather than asserted, which institutional buyers increasingly require in procurement.

ISO9001:2015

Quality management (cert. H3CR9TCU20251212INDQM10N)

Our certified quality system governs how work is run, recorded and released.

How It Works

How a Project Works

Every project follows the same four steps. The standard the work is held to depends on your audience.

Step one

A free first step

A sample edit, guideline check, feasibility assessment or gap analysis carried out on your own material.

Step two

Scope and quotation

We recommend the service you need, and we tell you when a less expensive option is sufficient.

Step three

Delivery of the work

Work is assigned by subject and built to the standard your destination sets, with the version named.

Step four

Handover of files

Code, models, search strategies and working documents are handed over so you can meet later deadlines independently.

FAQs

Frequently Asked Questions

If your question is not answered here, ask an expert — no quote is required.

Use the service menu, which is organised by type of work. It offers the same services, and many clients prefer it.

The audience pages are a shortcut for clients who know which group they belong to. They do not replace the service catalogue.

This is common. For example, a clinician-researcher at a university running an investigator-initiated trial belongs to four of these groups.

Start with the page that best describes your current piece of work. The services are the same whichever page you choose.

Because some services have a unit and some do not. Editing has a per-word rate. An HTA dossier or a clinical evaluation report does not, and publishing a number for one would be misleading.

Where a price is published, it is a starting price with its scope stated beside it.

Yes. One team assigns work by subject: a cardiology trial goes to a specialist familiar with the relevant CONSORT extension, and a device file goes to a specialist who works to MDR.

Work is assigned by subject rather than by account size, which is the part that matters to a single author.

Related services

Browse Services by Type of Work

The service menu lists each service by name.

Discuss Your Project to Find the Right Service

Describe your project and we will recommend the right service, including when a smaller service meets your needs.

Get a free quote

Regulations

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  1. 1Your work
  2. 2Your details
  3. 3Send
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Material you send is held under signed confidentiality, with access limited to the assigned team and encrypted transfer. It is not used to train anything and is not passed to third-party tools. Ask for the agreement before you send anything you would rather cover first.