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“A/end ZIL)Q, “ETHICSCOMMITTEE OF GLOBALBARODAHOSPITAL pvt. LRD.) (A UN TOF BARODAMEDTCAREDATE:20May2011 TO, DR.SEEMS BHATWADEKAR GlobalBarodaHosoital. NR. Shreya vidhyalaya, Jabalpur, Vadodara39O
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How to fill out clinical trials registry

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How to fill out clinical trials registry

01
First, gather all the necessary information about your clinical trial including the protocol, eligibility criteria, and study design.
02
Next, visit the official website of the clinical trials registry where you want to register your trial.
03
Create an account on the website if required, and log in to your account.
04
Locate the option to 'Submit a new trial' or similar, and click on it.
05
Fill out the registration form, providing accurate and complete information about your trial.
06
Make sure to include details about the study objectives, methodology, interventions, and outcome measures.
07
Attach any relevant documents such as the study protocol and informed consent forms.
08
Review the information you have entered carefully to ensure accuracy.
09
Once you are satisfied with the form, submit it for review.
10
Wait for the registry administrators to review your submission and provide feedback or approval.
11
Make any necessary revisions or provide additional information as requested.
12
Once your trial is approved, it will be assigned a unique identifier in the registry.
13
Keep a record of this identifier for future reference and dissemination of trial results.

Who needs clinical trials registry?

01
Researchers conducting clinical trials need the clinical trials registry to ensure transparency and accountability in their research activities.
02
Funding agencies and ethics committees may also require researchers to register their trials to ensure compliance with regulations and guidelines.
03
Healthcare professionals and other researchers can benefit from the clinical trials registry by accessing information about ongoing and completed trials.
04
Patients and patient advocacy groups can use the registry to find relevant clinical trials and make informed decisions about their healthcare options.
05
Policy-makers and regulatory authorities may utilize the clinical trials registry to monitor research trends, evaluate the impact of interventions, and inform policy decisions.
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Clinical trials registry is a database of clinical trials information that is publicly available and accessible to researchers, healthcare providers, and the general public.
Researchers and organizations conducting clinical trials are required to file clinical trials registry to ensure transparency and accessibility of trial information.
Clinical trials registry can be filled out online through the designated registry platform by providing detailed information about the trial protocol, study design, and outcomes.
The purpose of clinical trials registry is to promote transparency, accountability, and public trust in clinical research by providing access to information about ongoing and completed trials.
Information such as trial protocol, study design, participant eligibility criteria, outcomes, and results must be reported on clinical trials registry.
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