T A E T

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Trial Adverse Events Tracker (TAET)

Trial Adverse Events Tracker is an innovate technology platform aiming to enhance and improve tracking of adverse events and/or side effects for patients in clinical trials. The platform is designed to allow patients to instantly update investigators with adverse events they are experiencing onto an online database for trial investigators to keep informed on their patients.

 

COMING SOON  

 

Phases of Clinical Trial

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Phase 1

    Evaluate Safety Determine Safe Dosage Identify Side Effects

     

     

Approximately 70% of drugs move to the next phase

Phase 2

      Test Effectiveness Further Evaluate Safety

       

       

       

    Approximately 33% of drugs move to the next phase

Phase 3

      Confirm Effectiveness Monitor Side Effects Compare to Other Treatments Collect Information

    Approximately 25%-30% of drugs move to the next phase

Phase 4

      Provide Additional information after approval including risk, benefits, and best use

       

       

     

Clinical Trials State of the Industry

Research Institute & PPP Projects

CROs

FDA & Other regulatory bodies

Healthcare providers

Get Started

Trial Adverse Events Tracker (TAET)

Trial Adverse Events Tracker is an innovate technology platform aiming to enhance and improve tracking of adverse events and/or side effects for patients in clinical trials. The platform is designed to allow patients to instantly update investigators with adverse events they are experiencing onto an online database for trial investigators to keep informed on their patients.

  • Provide patients with superior national service
  • Patient access through user friendly app, update investigators
  • Provide investigators ability to chat with users in trial
  • Deliver exceptional pharmacy services from anywhereMake money security and control easier

Trial Benefits of TAET

Clinical trials are often done in 4 phases. Each phase has a different purpose and helps researchers answer specific questions.

What is an Adverse Event?

Adverse event means any untoward medical occurrence associated with the use of a drug in humans, whether or not considered’ drug related.

Creating a Trial
with TAET

Adverse event means any untoward medical occurrence associated with the use of a drug in humans, whether or not considered’ drug related.

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TAET’S Comprehensive Tracking Model

Adverse event means any untoward medical occurrence associated with the use of a drug in humans, whether or not considered’ drug related.

 


 

Future Clinical Studies

Effectiveness of a Computerized Cognitive Training Program for Reducing Head Impact Kinematics