18
YEARS
msCRO is a professional scientific solution partner for physicians, academics, clinical researchers and healthcare-sector research teams across clinical research, biostatistical analysis, medical writing, data management and SCI/SCI-E publication processes.
Comprehensive solutions from study design to advanced statistical analysis.
Experienced and reliable CRO support across clinical research processes.
Professional support in data collection, management and quality control.
We prepare your scientific content to international standards.
End-to-end strategic and applied support in your SCI/SCI-E publication process.
Scientific content and presentation support for your oral and poster abstracts.
Research-oriented advanced analysis with machine learning, radiomics and model validation.
18 years of academic experience in biostatistics, medical writing and the SCI/SCI-E publication process.
academic studies and clinical research supported
cities with research experience
institutions / hospitals collaborated with
medical and clinical specialties
different service types
international projects from Belgium supported
years of academic publication and analysis experience
Since some projects involve more than one service component, these shares are not a total distribution.
Experience in academic studies, clinical research and publication across more than 50 medical/clinical specialties.
Alongside its broad experience across Türkiye, Medical Statistic CRO has also provided biostatistics, medical writing and publication process support to academic and clinical research projects from Belgium.
Figures are compiled in anonymized form from the academic studies, clinical research, thesis-to-article conversions, biostatistical analyses, medical writing, journal selection and publication-process projects Medical Statistic CRO has supported to date.
Our ExperienceWe do not only analyze your data; we evaluate your hypothesis, methodology, data structure, academic framework, and publication objective together.
In scientific research, strong results are not achieved through data analysis alone. The right hypothesis, a sound methodology, an appropriate statistical approach, academic integrity, ethical responsibility and a publication strategy must be managed together.
By evaluating all the scientific components of research together, msCRO offers a holistic consultancy approach that makes studies not merely analysed but methodologically defensible, academically strong and better prepared for the publication process.
Each study is evaluated not only on the existing data set but by considering the research question, hypothesis, methodology, sample structure, variables, analysis plan and publication goal together. In this way the study is not merely analysed but made more scientifically consistent and defensible.
Statistical methods appropriate to the type of research, the data structure and the endpoints are determined. Analyses are planned, performed and reported not just to produce p-values but to answer the study’s scientific question correctly and meaningfully.
At msCRO, studies are not treated merely as converting existing material into article format. The introduction, methods, results, discussion and conclusion sections are structured to make the scientific value of the study visible, to be better prepared for peer review and to comply with academic publication standards.
A study’s areas for improvement are shared as openly as its strengths. No publication or acceptance is guaranteed; instead, the focus is on improving the scientific quality of the study, addressing methodological gaps and preparing it more strongly for the publication process.
Each project is handled with the attention and diligence its field of expertise requires. Different areas of expertise in biostatistics, clinical research methodology, medical writing, data science and academic publication processes are brought together and carried out with a teamwork and quality-control approach.
Scientific support is provided at critical stages of the publication process such as journal selection, manuscript submission, evaluation of reviewer comments, structuring revisions and preparing response letters. The aim is to contribute to preparing the study for publication as strongly as possible while preserving its academic integrity.
Researcher data, study files and academic content are handled with confidentiality and ethical responsibility. Each project is carried out with a secure working approach that respects the researcher’s effort and scientific ownership.
Let us evaluate your study scientifically.
You can start a preliminary assessment process for your manuscript, thesis, clinical research, product study or advanced analysis project.
Study objectives, data structure, methodological requirements, study design and project goals are comprehensively evaluated by our expert team.
Study methodology, protocol, Statistical Analysis Plan (SAP), sample size, data management and the overall project roadmap are developed in accordance with international standards.
Data undergo quality control procedures, biostatistical analyses and advanced analytics are performed, and analytical outputs are prepared for scientific reporting.
Medical writing, publication development, editorial planning, tables, figures and publication documentation are developed in accordance with international publishing standards.
Journal selection, manuscript submission, peer review management, technical documentation and final project deliverables are coordinated professionally.
You can work with msCRO at different stages of the research lifecycle, from research concept development, study design and protocol planning to sample size determination, data management, biostatistical analysis, advanced analytics, medical writing, publication development and peer-review revisions. Starting at an early stage supports alignment between methodology, data collection and the statistical analysis strategy. Projects with existing datasets or scientific documents can also be evaluated according to their scope and requirements.
Yes. msCRO provides services remotely to researchers, universities, healthcare organizations, pharmaceutical and biotechnology companies, medical device manufacturers and CROs in Türkiye and internationally. Preliminary assessments, meetings, project planning, secure data sharing, statistical analysis, medical writing, publication development and revision processes can all be managed through secure digital communication platforms. Face-to-face meetings may also be arranged when required.
The process begins with a preliminary assessment. Our experts evaluate the study objectives, research design, available data, existing documentation and project requirements. Based on this evaluation, the project scope, workflow, timeline and roadmap are established. The project then progresses through structured stages including research design and planning, data management and analysis, publication development and publication process management.
Statistical methods are selected according to the research objectives, study design, data structure, variable characteristics, study endpoints and research hypotheses rather than from a predefined list. Depending on the project requirements, analyses may include parametric and non-parametric methods, regression models, survival analysis, ROC analysis, mixed-effects models, machine learning, artificial intelligence applications and other advanced analytical approaches. Method selection is performed within the framework of the study methodology and the Statistical Analysis Plan (SAP).
No. We provide professional support throughout the publication process, including journal selection, publication strategy, medical writing, publication development, statistical review, technical editing and peer-review revisions. However, editorial decisions and manuscript acceptance are made solely by the journal's editors and independent reviewers. Therefore, publication acceptance in any specific journal or any particular publication outcome cannot be guaranteed.
Yes. We provide publication development support for completed thesis studies intended for submission to international scientific journals. The study methodology, statistical analyses, scientific reporting, medical writing, journal requirements and publication strategy are evaluated together to develop publication-ready scientific documentation. The process is based on the existing research data, scientific content and author contributions contained within the thesis.
msCRO places great importance on the confidentiality of personal data and project documentation. Information and documents shared with us are processed only for the purpose of delivering the requested services, by authorized personnel and in accordance with confidentiality obligations. Appropriate technical and organizational safeguards are applied to protect data, and research datasets are encouraged to be shared in anonymized or coded form whenever possible. Further information is available in our Privacy Policy and Personal Data Protection Notice.
Pricing is determined individually for each project based on its scope, study design, data structure, requested services, technical requirements, estimated workload and delivery timeline. Following the preliminary assessment, the project scope is clarified and a detailed quotation is prepared. If the project scope changes during the process, the quotation may be revised with mutual agreement.
Start your preliminary assessment with our expert team for clinical research, academic projects, biostatistics, data management, medical writing, publication development and integrated CRO solutions.
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