Targeted literature searches are a fundamental part of writing clinical manuscripts that will meet the standards of high-quality journals and contribute meaningfully to evidence-based practice. When physicians write clinical manuscripts, utilizing a targeted literature search can identify high-quality, relevant, and current evidence. While a general literature review is useful, a targeted literature search is specific to the clinical question and should be completed through frameworks established, such as PICO (Population, Intervention, Comparator, Outcome) and PRISMA [1].
Medically oriented and scientific writing are two basic types of communication used in research and health industries. Often these two terms are used interchangeably; however, these two types of writing consist of different objectives, audiences and format conventions. Understanding the differences between these two types of writing is crucial for people involved in academic writing, clinical reporting, publication writing, or regulatory writing.
This article will identify the primary differences between scientific and medical writing in terms of style, structure, language, audience, and purpose, and will lend some clarity to the sharing of information between medical and scientific writing. [1]
The main purpose of scientific writing is to share new knowledge, hypotheses, or experimental results in an accurate, reproducible way. Scientific writing relates mainly to the academic/research world.
Medical writing presents clinical facts, outcomes of treatment, or regulatory information with a focus on the healthcare professional, regulatory agency, or the patient.
In general, scientific writing follows an IMRaD format (Introduction, Methods, Results and Discussion), while medical writing can refer to many documents—clinical study reports, regulatory dossiers, patient information leaflets, and continuing medical education (CME) documents, just to name a few.
| Feature | Scientific Writing | Medical Writing |
|---|---|---|
| Primary Goal | Share research findings | Communicate clinical, regulatory, or educational content |
| Audience | Researchers, scientists, journal editors | Clinicians, regulatory agencies, patients |
| Tone | Objective, analytical, and formal | Clear, patient-centric (or technical for regulatory) |
| Structure | IMRaD format | Varies: clinical study reports, drug monographs, brochures |
| Compliance | Academic integrity and ethics (e.g., COPE) | Regulatory compliance (e.g., FDA, ICH-GCP) |
| Publication | Academic journals | Regulatory submissions, medical journals, or healthcare media |
| Language Complexity | High (discipline-specific terms) | Balanced technicality and readability |
| References | peer-reviewed sources | Clinical trial data, regulatory guidelines |
| Types of Output | Journal articles, white papers, research reports | Clinical Protocols writing, regulatory documents, CME slides, patient leaflets |
| Scientific Writing: | Medical Writing: |
|---|---|
| Research articles | Clinical trial protocols |
| Meta-analyses | Investigator brochures |
| Systematic reviews | Summary of Product Characteristics (SmPC) |
| Theses and dissertations | Informed consent forms |
| Technical reports | Medical communication and education content |
Both writing styles will require a focus on accuracy, transparency and clarity. Scientific writing tends to be logic-based where a hypothesis drives the writing and reproducibility is essential, while medical writing requires patient safety, compliance and transparency regarding clear benefit and risk. [4]
Professional writing services, such as PhD Scientific Manuscript Writing Support or Medical Regulatory Writing Services, lend themselves to content creation that adheres to often narrow quality boundaries for researchers, Clinicians, and pharmaceutical companies to achieve their publication or compliance objectives.
Scientific writing and medical writing both of which play important roles in advancing knowledge and improving health care are distinct in purpose, form and audience. Bridging the two is important and ensures clear codes once made, compliance, and ways to advance information in various domains through effective communication. Writers are obligated to change the tone, style and content to meet the end-user’s needs in either situation (journal article or application submission dossier).
Bridging the Gap: Key Differences Between Scientific and Medical Writing? Pubrica offers end-to-end research design, analysis, and reporting support.