American SciTech International-CRO Electronic Data Capture System:

ASI-SYS (American SciTech International - Systems) is web based CLINICAL DATAMANAGMENT SYSTEM. It is still in process of upgrading and expanding to optimize our networking and business. It is fully compliant with 21 CRF Part 11 regulations. All components of the System are fully integrated to reduce errors in capturing clinical trial data. It is secured and safe to maintain the data integrity and analysis of high volume and complicated study projects. This system gives accurate and secure access to our project management team. Our industrial and non industrial sponsor clients can access ASI-SYS for on-line review of status and the progress of their clinical trial projects around the clock. It is a highly efficient and intricate system to keep track of the safety of our research subjects.

Special attention is given to:

• Serious Adverse Events
• Accuracy of data
• Meeting Deadlines
• Effortless communication among Investigators, (Sites), IRBs, Sponsors; CROs and the Pharmaceutical companies

These excellent strategies will help clinical researchers and committed teams to address question that are not answered at the time of enrollment. It address actual safety issues of subjects, and provides an effective plan for clinical trials in the globally spread competitive world.

Ready work force for Monitoring: Most of our CRAs are trained EDC and to communicate through ASI-SYS. The CRAs have a strong medical background with an average experience of 8-10 years. They are primarily medical graduates, dentists, pharmacists, nurses and scientists.

We have multiple teams of CRAs, who participate in the dedicated and specialized work of clinical research. They are divided on the basis of therapeutic areas of study, clinical trial phases, and previous educational background.