Medical Writing
Evidence-based medical writing and analysis for review
We organise medical writing and analysis around the available materials, intended use and professional review requirements, covering development stages from target discovery to post-marketing. Services are grouped into Medical Affairs, research publications and clinical development. Evidence and statistics, and medical review and quality control, are specialist services that can also be commissioned separately.
Authorship and final responsibility rest with the client; individual authorship eligibility is determined under the applicable publication standards.
- 2 + 2 rounds
- 2 + 2 roundsAt least 2 rounds of internal quality control, plus 2 rounds of client revisions.
- 24 hours
- 24 hoursto reply (business days first).
- Team and therapeutic areas
- 14 professionals; 5 of them currently hold 17 journal editorial roles.View team informationView therapeutic areas
01Medical Writing
Find services by area
The same research data require different document types for different readers. Choose an area by the intended use of your document, or search by document name for service scope and delivery requirements.
Medical affairs and medical education
We organise scientific content around clinical questions, keeping conclusions and their qualifications linked to the original sources.
Research publications
We organise publication plans, manuscripts and conference materials, keeping methods, results and conclusions consistent.
Clinical development and regulatory submissions
We integrate study materials and analysis outputs into drafts for review in the required document format. The scope of the engagement is confirmed before quotation.
Evidence and statistics
We conduct literature searches, evidence synthesis and statistical analysis, including target evidence and preclinical experimental statistics, with methods and results available for verification.
Medical review and quality control
We independently review a specified version, checking numerical accuracy, interpretive limits and the handling of review comments.
02Medical Writing
Delivery process and quality control
We confirm the delivery scope first, separate writing and quality control responsibilities, and record review comments individually.
The requirement confirmation form specifies the stage of involvement, deliverable definitions and counting rules, the materials list and authorisation status, and the project schedule. Standard provision includes at least 2 rounds of internal quality control plus 2 rounds of client revisions. Delivery includes a point-by-point record of responses to comments.
Medical writing support uses tailored quotations; the three Clinical Research Services packages do not apply.
View team information03Medical Writing
Selected samples
The following illustrative samples show document structures and presentation formats. They do not represent client projects or a regulatory submission track record.
Figure caption
Illustrative sample. Shows slide formats for scientific content and key data.
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Illustrative sample. Shows the chapter structure of a clinical study report.
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Illustrative sample. Shows how claims are linked to their sources.
Get started · Submit a request
Submit a medical writing request
Please provide document types, quantities, the current stage, intended use, available materials and deadlines. We first issue a requirement confirmation form, followed by an itemised quotation and schedule.
This section describes our services. It does not concern any specific medicinal product and does not constitute drug advertising. The stated timelines, quality control and resolution procedures reflect standard working practices. Final deliverables, timelines, prices and each party's obligations are governed by the contract signed by both parties.
Writing and statistical support for research publications follows the recommendations of the International Committee of Medical Journal Editors (ICMJE) and Good Publication Practice 2022. Our contribution is disclosed in the acknowledgements in line with ICMJE and GPP 2022; we are not listed as authors. Funding sources are also disclosed truthfully. We do not promise publication outcomes.