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Project Management

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
• Post Marketing Research Trial
• Feasibility Evaluations and Site Selection Process
• Data Management
• Statistical Analysis
• CROSS (Clinical Research Organization Software System)


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-  Besides  conducting  all  of  these we  handle  essential  trial  documents  by  using   CROSS.  AlfaCRO   provides  online document management, e-CRF designs,  and database security.