In project management ensuring compliance through ICH-GCP guidelines, effective planning and analytic approach, AlfaCRO exceeds expectations through clinical trials of Phase I -IV. Furthermore, our main manner of business managing is to conduct all of these steps accurately due to project features. In the scope of project management services, AlfaCRO provides management of all aspects of a clinical trial starting from even e-CRF design or IEC & MoH / IRB submissions until the final statistical analyses of project database. Through all these processes AlfaCRO uses the latest technology in the most innovative way. You may choose to partner up with AlfaCRO for;
- Phase I-IV Clinical Trials
- Medical Device Trial
- Submission Support :We are supporting to your study at the start up for Ministry of Health and Ethic Committe submission and aproval process, follow up, query answers and finalise the approval process.
- Post Marketing Research Trial
- Feasibility Evaluations and Site Selection Process : AlfaCRO provides careful and effective selection and evaluation procedure for research sites based on both the needs of clinical trial itself experience.
- Data Management : AlfaCRO data management results in unbiased and unfabricated trial database with minimum queries to solve.
- Statistical Analysis: AlfaCRO provides fast and reliable results of statistical analysis of your clinical trial database using most up to date technology.
- CROSS (Clinical Research Organization Software System) : Besides conducting all of these we handle essential trial documents by using AlfaCRO provides online document management, e-CRF designs, and database security.