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Presents14th Annual Clinical Trials Summit 2023#Vista critical guide for successfully conducting Clinical Trials23rd 24th May 2023, Kohinoor Continental Hotel, Mumbai India AGENDA AT A GLANCE Key
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01
Go to the clinicaltrialsgov website
02
Log in with your account credentials
03
Click on 'Create a new study recordbeta' link
04
Fill out the required fields such as study title, study description, study design, and study status
05
Upload any relevant documents or files related to the study
06
Review the information you have entered before submitting the study record

Who needs study recordbeta clinicaltrialsgov?

01
Researchers conducting clinical trials who want to register and manage their studies in a public database
02
Participants looking for information about ongoing or completed clinical trials for research purposes
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Study recordbeta ClinicalTrials.gov is a publicly accessible database that provides information on clinical trials.
Researchers conducting clinical trials are required to file study recordbeta ClinicalTrials.gov.
To fill out study recordbeta ClinicalTrials.gov, researchers must provide information such as study design, interventions, eligibility criteria, and study timeline.
The purpose of study recordbeta ClinicalTrials.gov is to increase transparency and promote access to information about clinical trials.
Information such as study title, principal investigator, study objectives, outcome measures, and recruitment status must be reported on study recordbeta ClinicalTrials.gov.
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