Ratio Medica MEDICAL WRITING
MEDICAL WRITING · CLINICAL RESEARCH · DATA ANALYSIS

Rigorous scientific documentation

We prepare medical articles and texts, clinical trial documentation and analyses of study results. We work to international standards, backed by the expertise of a full professor and active researcher.

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ICH‑GCP E6(R3)ICH E3CONSORTSTROBEPRISMAICMJEGPP 2022MDREU CTR 536/2014
ProfessorPhD, DSc (habil.)
21years in research
91peer‑reviewed publications
250+citations
SERVICES

How we can help

We combine writing craft with a researcher’s expertise. We understand methodology, statistics and regulatory requirements, so every text is accurate not only in its language but in its substance.

01

Medical articles and texts

Manuscripts tailored to your target journal and ready for peer review.

  • Original research and review articles
  • Systematic reviews and meta‑analyses
  • Scientific and language editing
  • Responses to reviewers
  • Grant applications
  • Educational materials
02

Clinical trial documentation

Documents compliant with ICH‑GCP and the requirements of ethics committees and regulators.

  • Study protocols and amendments
  • Investigator’s Brochure
  • Informed consent forms
  • Statistical analysis plan (SAP)
  • Clinical study report (CSR)
  • Clinical evaluation report (CER)
03

Analysis of study results

Clear analysis and interpretation of data — for reviewers, sponsors and patients.

  • Statistical analysis
  • Interpretation of results
  • Tables, charts and figures
  • Plain language summaries
  • Sponsor reports
WHO WE WORK WITH

Who we work with

Pharmaceutical companies and CROsTrial documentation and sponsor reports
Medical device manufacturersMDR‑compliant clinical evaluation
Physicians and research teamsPublications, data analysis, grants
Hospitals and universitiesSupport for research projects
HOW WE WORK

A transparent process, clear deadlines

  1. STEP 01Free consultationWe learn about your project and its goals. On request, we sign a non‑disclosure agreement before you share any materials.
  2. STEP 02Quote and timelineYou receive the scope of work, deadline and price — with no hidden costs.
  3. STEP 03DraftingWe work in stages and review every draft with you.
  4. STEP 04Delivery and supportWe deliver the final version and help you respond to reviewers’ comments.
Start with a free consultation
Prof. Marta Majorek
ABOUT

Ratio Medica is built on a scientist’s experience, not just a writer’s

Our work is led by Prof. Marta Majorek, PhD, DSc — a researcher, author and peer reviewer for reputable scientific journals. Every day she designs studies, analyses their results and evaluates the work of other scientists.

That is why we know what reviewers, ethics committees and sponsors expect — and we prepare texts that meet those expectations the first time.

ORCID profile → Google Scholar profile →
CONTACT

Tell us about your project

We reply within 2 business days. The first consultation is free and without obligation.

E‑MAIL[email protected] PHONE+48 692 435 588

Privacy policy

1. Who is the controller of your data

The controller of your personal data is Marta Majorek, trading as Ratio Medica, [address and tax ID — to be added once the business is registered]. For any matters concerning personal data, you can write to [email protected] or call +48 692 435 588.

2. What data we process

  • Contact form data: full name, email address, type of project, expected deadline and project description.
  • Correspondence data: any data you share with us by email or during a phone call.
  • Technical data: IP address, browser type and time of visit, recorded automatically in the logs of the server hosting the website.

3. Purposes and legal basis

  • Responding to your enquiry and preparing a quote — steps taken at your request before entering into a contract (Article 6(1)(b) GDPR) and your consent given in the form (Article 6(1)(a) GDPR).
  • Performing a contract (Article 6(1)(b) GDPR).
  • Handling correspondence, keeping the website secure and establishing, exercising or defending legal claims — our legitimate interest (Article 6(1)(f) GDPR).
  • Meeting tax and accounting obligations if we work together (Article 6(1)(c) GDPR).

4. How long we keep data

  • Enquiries that do not lead to a contract — up to 12 months from the last contact.
  • Contract-related data — for the duration of the contract and then until the relevant limitation periods and statutory tax retention periods expire.
  • Server logs — for a short period set by the hosting provider.

5. Who we share data with

We do not sell your data or share it for marketing purposes. Data may only be disclosed to providers who technically support our business: the website hosting provider, the email provider, the contact form service provider and our accounting office. They process data on our behalf and in line with the GDPR.

If any provider processes data outside the European Economic Area, this is based on a European Commission adequacy decision or standard contractual clauses.

6. Patient and study participant data

Please do not send, via the form or in your first message, any data that could identify patients or study participants. If a project requires processing such data, we sign a separate data processing agreement (Article 28 GDPR). All materials shared in connection with a project are treated as confidential, and we sign a non‑disclosure agreement on request.

7. Your rights

You have the right to:

  • access your data and receive a copy,
  • rectify your data,
  • have your data erased or its processing restricted,
  • data portability,
  • object to processing based on legitimate interest,
  • withdraw your consent at any time, without affecting the lawfulness of processing before withdrawal,
  • lodge a complaint with a supervisory authority — in Poland, the President of the Personal Data Protection Office (UODO, ul. Stawki 2, 00‑193 Warsaw), or the authority in your country of residence or work.

To exercise your rights, write to [email protected].

8. Do you have to provide data

Providing data is voluntary, but without an email address or phone number we will not be able to reply to your enquiry. We do not make automated decisions or profile users.

9. Cookies and browser storage

This website does not use tracking cookies or analytics tools. The only information saved in your browser’s storage (localStorage) is the language version you choose — we save it only when you click the PL / EN switch, so that the right version is shown on your next visit. You can remove it by clearing the site data in your browser settings.

Fonts are stored on our own server, so the website does not connect to Google servers. Links to the ORCID and Google Scholar profiles lead to external services with their own privacy policies.

10. Changes to this policy

We may update this policy, for example following changes in the law or in how the website works. The current version is always available on this website.

Last updated: 1 October 2026