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2024-04-29 |
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We will start the activities for you by receiving the necessary documents from
you, including the study protocol. The details are established during the
meeting/discussion. Note: it is not necessary for you to provide your CRF, we
can prepare it for you based on our knowledge and experience.
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The day after transfer of the needed trail documents |
At this point, you will receive a demo version of the eCRF system developed from
the data provided by you. Then we begin the stage of detailing the eCRf content
to ensure the highest possible data quality.
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Not later than two weeks from the beginning of the implementation
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Not later than one month from the beginning of the implementation
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This is the duration of the planned study, such as 3 years, 5
years, etc.
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If your request is urgent, please mark it in the form.
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The approximate date of the start of the study, may change later.
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If randomization is planned in your study select it from the list. If a
particular method is not listed here, then write us about it in the comments, or
inform us at the meeting
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Fill in the approximate number of users, including all roles - researchers,
coordinators, Monitors, and Sponsors. This will help us properly estimate the
price of the product for you.
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We have extensive experience in integrating the IWRS module with eCRF which
allows for the error-free management of medication for patients. If your study
requires IWRS, please select this option.
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If your study collects any digital data,
including test results in text/number or image form, we can prepare a data repository for you that will be connected to the eCRF.
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Write your comment here,
all the necessary information that will help us prepare an offer best suited to your needs.
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