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Get the free CReST Randomisation notepad

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This form is to be completed for randomising patients into the CReST study and requires patient information, eligibility checklist, and randomisation details.
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How to fill out crest randomisation notepad

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How to fill out CReST Randomisation notepad

01
Obtain a CReST Randomisation notepad from the study coordinator.
02
Write the study identifier and participant's initials on the cover page.
03
Number each page consecutively as per the participant's randomisation number.
04
Follow the randomisation sequence provided in the notepad for participant allocations.
05
Record the assigned treatment for each participant on the designated page.
06
Ensure that all entries are clear and legible to maintain accurate records.
07
Sign and date the completed pages to verify the accuracy of data recorded.

Who needs CReST Randomisation notepad?

01
Clinical trial coordinators and investigators managing participant allocation need the CReST Randomisation notepad.
02
Research teams conducting randomised clinical trials will require the notepad for documentation.
03
Regulatory personnel may need to review the notepad for compliance with randomisation protocols.
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CReST Randomisation notepad is a tool used in clinical trials to ensure that participants are assigned to either the treatment or control group randomly, thereby minimizing bias in the study results.
Investigators and trial coordinators involved in clinical trials that require randomisation are required to file the CReST Randomisation notepad.
To fill out the CReST Randomisation notepad, researchers must record the method of randomisation used, the allocation sequence, and details of participant assignments along with any relevant dates and identifiers.
The purpose of the CReST Randomisation notepad is to provide a transparent and reproducible record of the randomisation process, ensuring the integrity and scientific validity of the clinical trial.
The information that must be reported on the CReST Randomisation notepad includes the randomisation method, allocation sequence, dates of randomisation, participant identifiers, and any deviations from the planned randomisation process.
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