Services
We provide a wide range of Services tailored to your need
Our team of experienced medical specialists, statisticians, and writers is dedicated to delivering high-quality research, systematic reviews, meta-analyses, and clinical trial designs to meet your scientific and regulatory needs.
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EviSync is committed to advancing research and compliance by providing a comprehensive range of services, including evidence synthesis, systematic literature reviews, meta-analyses, and clinical trial design.
Regulatory and Scientific Writing
- Protocols for Systematic Reviews and Clinical Trials
- Manuscript for Scientific Journals Submission
- Regulatory Submissions (FDA, EMA, MHRA)
- Scientific Reports
- Performance Reports
Systematic Literature Review
- Define Research Questions using PICO Framework
- Systematic Search Strategies in Multiple Databases
- Study Screening & Selections
- Quality Assessment Including Risk of Bias (RoB)
- Quantitative and Qualitative Data Synthesis
- Addressing Publication Bias
- Assess the Quality of the Evidence using GRADE
Meta-analysis
- Data extraction
- Select the Outcome Measures
- Choose the Model for Meta-analysis (Random vs Fixed)
- Effect Size Calculation (MD, SMD, OR, RR)
- Heterogeneity Assessment (Q-test)
- Forest Plots Generation
- Funnel Plots Generation
- Subgroup Analysis
- Sensitivity Analysis
- Results Interpretation and Reporting (PRISMA)
Clinical Trial Designs
- Study Concepts and Development
- Phase 1-4 Trial Design and Planning
- Statistical Design and Sample Size Calculation
- Regulatory and Ethical Compliance
- Site and Investigator Selection
- Endpoint Selection and Validation
- Risk Management and Quality Assurance
- Patients Recruitment and Retention Strategies
- Statistical Analysis
- Results Interpretation and Reporting
Data Management
- Data Collection and Organisation
- Database Design and Maintenance
- Data Cleaning and Validation
- Data Coding and Standardisation
- Real-time Data Monitoring
- Data Integration and Analysis
- Documentation and Reporting
Training and Workshops
- Systematic Reviews and Meta-analyses
- Clinical Trial Design and Management
- Evidence Synthesis
- Search in the Databases
- Scientific and Regulatory Writing
- Resaerch Methodology and Statistical Analysis
- Data Management and Visualisation
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