About Us
Integrated CRO and Data Science Solutions for Scientific Research
msCRO (Medical Statistic CRO) is an independent scientific research organization providing CRO solutions in clinical research, biostatistics, clinical data management, research methodology, medical writing, publication development and advanced data analytics.
Since 2008, we have worked with investigators, universities, healthcare organizations, research institutions, pharmaceutical and biotechnology companies, medical device manufacturers and CRO teams to strengthen the methodological, statistical and scientific quality of clinical and academic research.
We do not view research merely as a dataset to be analyzed, a report to be completed or a publication submission to be processed. We consider the research question, study design, data management, biostatistical analysis, medical writing and publication management as interconnected components of a comprehensive scientific process.
Through this integrated approach, we establish a coherent research framework connecting the clinical objective, methodological structure, data sources, study endpoints, analytical strategy and intended scientific outputs.
Integrated Research Approach
The quality of scientific research begins to take shape during the earliest stages of planning, not only when the data are analyzed. Clearly defining the research question, selecting an appropriate study design, identifying clinically meaningful endpoints, determining the required sample size and aligning data collection procedures with analytical requirements are fundamental to generating reliable scientific evidence.
msCRO approaches research methodology, clinical data management, biostatistics, advanced analytics, medical writing and publication development not as isolated services, but as complementary elements of the same research lifecycle.
Each project is evaluated within its own context, considering the study objective, design, target population, variable structure, data quality, statistical requirements and scientific communication goals.
Our Areas of Expertise
Our areas of expertise include:
- Clinical study design and research methodology
- Study protocols and scientific documentation
- Ethics committee and regulatory submission documentation
- Clinical project management and research coordination
- Clinical trial monitoring
- Clinical data management and CRF/eCRF solutions
- Statistical Analysis Plans
- Sample size determination and power analysis
- Biostatistics and advanced statistical modeling
- Machine learning, artificial intelligence and predictive modeling
- Radiomics and medical imaging analytics
- Medical writing and publication development
- Clinical study reporting
- Publication management and peer-review support
- Scientific congress and abstract services
These areas cover scientific and technical solutions for the planning, data management, analysis, reporting and publication development stages of clinical and academic research.
Scientific and International Standards
The methodological and scientific structure of our work is developed with reference to international guidelines and reporting standards relevant to the type and scope of each project.
Depending on project requirements, our work may draw on ICH-GCP, ICH E9, CONSORT, SPIRIT, STROBE, PRISMA, TRIPOD, STARD, CARE, RECORD, CHEERS, ARRIVE, ICMJE Recommendations, Good Publication Practice and the EQUATOR Network. For projects requiring standardized clinical data structures, CDISC, CDASH, SDTM and ADaM frameworks may also be considered according to project scope.
This approach supports methodological consistency across study design, data structure, analytical strategy and scientific reporting.
Multidisciplinary Expertise
Clinical and scientific research requires the integration of methodology, clinical knowledge, data management, statistics, scientific communication and publication expertise.
Projects are conducted with contributions from specialists in biostatistics, data science, clinical research methodology, medical writing, artificial intelligence, publication development and scientific editing, depending on their scope and technical requirements.
Each project is reviewed from a multidisciplinary perspective, with attention to methodological integrity, statistical appropriateness, data quality, scientific communication and publication strategy.
Our Medical Writing and Publication Development Approach
Our medical writing and publication development processes are based on research data, scientific materials, clinical and technical information and author or sponsor contributions.
Publication strategy, scientific document development, editorial planning, statistical reporting, table and figure development, journal selection, peer-review revisions and submission documentation are structured in accordance with international publication ethics and good publication practices.
This approach supports the development of scientific outputs that are clear, coherent, methodologically robust and aligned with the requirements of the intended publication format.
Our Approach to Quality
We do not define quality solely as an accurate statistical result or a completed document.
Quality is achieved through:
- clear definition of the research question,
- alignment of the study design with the scientific objective,
- standardized data collection and management processes,
- appropriate application of statistical methods,
- evaluation of model assumptions and results,
- clear and consistent scientific reporting,
- preservation of methodological integrity throughout the project.
Methodological, statistical, data-focused and editorial quality-control steps are applied according to the scope and requirements of each project.
A Trusted Scientific Solutions Partner
msCRO aims to provide sustainable scientific solutions across different stages of research rather than functioning solely as a provider of individual analyses or documents.
From research concept development and study design to clinical data management, biostatistical analysis, medical writing, publication development and publication process management, we create service models aligned with the specific requirements of each project.
Our working culture is built on scientific accuracy, methodological consistency, quality control, data security, transparent communication, ethical practice and continuous development.
Our Vision
To be a trusted CRO and scientific research partner that strengthens the quality of clinical and scientific research, integrates biostatistics and data science with robust research methodology and provides reliable solutions within national and international research environments.
Our Mission
To contribute to the development of reliable scientific outputs by providing researchers, universities, healthcare organizations and the life sciences industry with integrated solutions in research design, clinical data management, biostatistics, advanced analytics, medical writing and publication development.