Medical writing produces publication-grade and submission-ready documents that translate complex data into precise, readable text for scientific peers, regulators, and leadership teams. Work spans manuscripts for peer-reviewed journals, book chapters, clinical and observational study documents, protocol and statistical language prepared with biostatistics, and structured submission packages. Reporting follows journal instructions and accepted standards, including CONSORT for clinical trials, PRISMA for reviews, and ICMJE recommendations for authorship, disclosures, and data-sharing statements. Terminology is harmonised across sections and appendices.
Each assignment is anchored to a defined question, an agreed method, and a disciplined review cycle. Source material is organized into a searchable library with citation keys and persistent identifiers. Figures and tables are generated from verifiable data, legends are written to stand alone, and supplementary files are prepared so reviewers can trace each value to origin. When literature synthesis is required, search strategies and study-selection steps are documented, bias assessment is described, evidence is graded, and exclusion reasons are preserved for audit.
Manuscripts are positioned for the target journal with calibrated language, structured abstracts, and coherent narrative flow from background and objectives to methods, results, and interpretation. For company-authored work, internal terminology is aligned to external style without diluting scientific precision. Cover letters, author contribution statements, data availability notes, and conflict-of-interest disclosures are prepared to venue policy. Where appropriate, graphical abstracts and plain-language summaries are produced for wider readership. Response-to-reviewers documents are drafted with point-by-point mapping and tracked revisions.
Clinical and regulatory documents are written to the expectations of multidisciplinary reviewers. Protocols and statistical analysis plan text reduce ambiguity and anticipate common queries. Clinical and non-clinical summaries follow ICH conventions for structure, cross-references, and links from narrative to tables, listings, and figures. Assumptions are explicit, acronyms are controlled, and version history is preserved for audit.
Quality controls are embedded in drafting and revision. Claims are bounded by the strength of evidence; uncertainty is stated where material to decisions. Numerical values are checked for internal consistency across text, tables, and graphics. Citations are formatted consistently and validated against source metadata. Language editing focuses on clarity and economy while preserving technical meaning for cross-functional readers.
Delivery is predictable. Draft one is provided on the scheduled date with tracked changes and a comment log explaining key decisions and references. One focused revision round is included to close open questions and finalise the document. Handover includes the manuscript or report file, editable vector figures, and the managed bibliography. Work fits document-control and information-security requirements and integrates with common tooling for versioning and collaboration. Assignments are executed in English for organisations across Europe and beyond, with contracting and invoicing available in CHF, EUR, NOK, or DKK.
For scoping, share the objective, target venue or audience, deadline, applicable standards, and confidentiality requirements. A written statement of work will set the method, deliverables, schedule, and pricing as fixed or capped, with milestones aligned to internal governance.