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. 

msCRO provides integrated CRO solutions across the planning, data management, analysis, reporting and publication stages of clinical research and life sciences projects. Our expertise includes research methodology, clinical project management, clinical data management, biostatistics, sample size determination and power analysis, Statistical Analysis Plans (SAP), artificial intelligence and advanced analytics, radiomics, medical writing, publication development, publication management, peer-review support and scientific congress services. Our solutions are tailored for researchers, universities, healthcare organizations, pharmaceutical and biotechnology companies, medical device manufacturers, CROs and research institutions.

 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. 

 The completion time depends on the scope of the project, study design, available data, current project stage and the services requested. Following the preliminary assessment, a detailed project plan together with an estimated delivery timeline is shared with you. Where feasible, accelerated project schedules may also be arranged for time-sensitive projects. 

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).

 Yes. Sample size determination and statistical power analyses are performed according to the study design, research hypothesis, primary endpoint, expected effect size, variance or event rate, statistical power and significance level. Depending on the project requirements, G*Power, PASS, R, SAS and simulation-based methods may be used to prepare methodological reports suitable for ethics committee submissions, study protocols, research proposals and scientific publications. 

 The choice of statistical software depends on the study design, data structure and analytical requirements of each project. Our primary analytical platforms include R, Python, SAS, SPSS, Stata and, where appropriate, PASS and G*Power. For machine learning and advanced analytics projects, we may use TensorFlow, PyTorch, scikit-learn, XGBoost, LightGBM, CatBoost and related analytical libraries. Radiomics projects may also involve platforms such as PyRadiomics, SimpleITK and OpenCV. Software selection is based on the scientific and technical requirements of each study. 

 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. Appropriate journal options are identified by evaluating the study topic, methodology, scientific scope, target audience, publication strategy and indexing requirements. Recommendations are based on each journal's scope, editorial policies, review process and indexing status. The final journal selection and submission decision remain the responsibility of the author(s) and/or sponsor. 

 Yes. Reviewer and editor comments are evaluated from methodological, statistical and editorial perspectives. Where appropriate, additional analyses are planned, tables and figures are updated, scientific justifications are refined and support is provided for preparing Responses to Reviewers in accordance with international publication standards. Our goal is to support a structured and scientifically consistent revision process while maintaining the integrity of the research. 

 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. 

Yes. We provide scientific and technical support for the preparation of research protocols, scientific rationale, study methodology, Statistical Analysis Plans (SAP), sample size calculations, informed consent documentation, CRF/eCRF development and ethics committee submission packages. Submission documents are structured according to the study type and the requirements of the relevant ethics committee or institution. The review and approval process remains under the authority of the respective ethics committee.

 No. Authorship of scientific publications is determined according to internationally accepted authorship criteria and the scientific contributions made to the research. msCRO provides professional support in research methodology, biostatistics, clinical data management, medical writing, publication development and publication management. Decisions regarding authorship are made by the investigators and/or sponsor in accordance with internationally accepted publication ethics. 

 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.