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EMA OTIS SPONSOR USER TRAINING Program The New Way of Submitting, Managing and reporting a clinical trial via the Clinical Trial Information System Blended training course including on demand and

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Who needs clinical trials information system?

01

Researchers conducting clinical trials

02

Clinical trial coordinators

03

Regulatory bodies overseeing clinical trials

04

Healthcare professionals involved in clinical research

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What is clinical trials information system?

Clinical trials information system is a web-based system that allows researchers and sponsors to submit and track information related to clinical trials.

Who is required to file clinical trials information system?

Researchers and sponsors conducting clinical trials are required to file clinical trials information system.

How to fill out clinical trials information system?

To fill out clinical trials information system, researchers and sponsors need to create an account, input study details, upload required documents, and submit the information.

What is the purpose of clinical trials information system?

The purpose of clinical trials information system is to provide transparency and accountability in clinical trial research, and to ensure compliance with regulations.

What information must be reported on clinical trials information system?

Information such as study protocol, trial status, recruitment status, and results must be reported on clinical trials information system.

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