DETA CRO is a Contract Research Organization that provides all laboratory services within its own body and serves the industry with its professional staff, keeping the Volunteer safety in the forefront, in High Quality for Medical Device Companies, Pharmaceutical Companies, Health Organizations, Associations and Researchers in our country and abroad. Our services;
• Study Design
• Sample Size Calculation
• Clinical Protocol Writing, Preparation of Abstract, Adaptation, and Review • All Laboratory tests (Genetics, Cytology, Pathology, Hematology, Oncology, etc.) that should be checked as per the protocol
• Informed Consent Form Design (ICF) , Adaptation, Review
• Case Report Form (e-CRF, Paper CRF) Design, Adaptation, Review
• IXRS (Web-based Randomization System) Design
• Ethics Committee Application File Preparation
• Turkish Medicines and Medical Devices Agency Application File • Project Management
• Site Management
• Investigator Meeting Organization, Participation, Presentation
• Monitoring Service (Feasibility, Initiation, Follow-up, Close out, Remote)
• Site Organization Management (Clinical Research Nurse, Home Visit, Site Coordinator, Data Entry Support Personnel)
• Investigator Product Storage and Distribution
• Trial Documents Storage (e-TMF, paper TMF)
• Preparing Guidelines (Monitoring, Data, Communication, Project, Statistics-Analysis, etc.)
• Clinical Trial Contract Preparation, Follow-up, Approval (CTA)
• Public Hospitals Association Pre-authorization File Preparation, Follow-up, Approval
• Database Preparation, Data Entry, Data Analysis, Query Solution
• Clinical Research Report
• Article Writing
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