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Date of event 28.03.2015 04.04.2015 04.04.2015 11.04.2015 11.04.2015 11.04.2015 11.04.2015 11.04.2015 11.04.2015 11.04.2015 18.04.2015 18.04.2015 18.04.2015 18.04.2015 25.04.2015 25.04.2015 Starting
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How to fill out national trials stores:

01
Gather all necessary information: Before starting to fill out the national trials stores, make sure you have all the required information handy. This might include details about the trial, participants, locations, dates, and any specific requirements or instructions.
02
Understand the form structure: Familiarize yourself with the layout and structure of the national trials stores form. This will help you navigate through the different sections and provide information in the appropriate fields.
03
Start with basic details: Begin filling out the form by providing basic information such as the trial name, trial ID, and the name of the main investigator. These details are usually found at the top of the form and serve as identifiers.
04
Provide trial objectives and description: In the designated sections, clearly outline the objectives and description of the trial. This helps to provide an overview of the study and its purpose.
05
Fill in participant information: Include information about the participants, such as their demographics, medical history, and any prior participation in clinical trials. This helps researchers assess the suitability of individuals for the trial.
06
Detail trial procedures and interventions: Specify the procedures, interventions, and treatments involved in the trial. Provide clear instructions and explanations to ensure accurate documentation.
07
Record data collection methods: Indicate how data will be collected, documented, and stored during the trial. This may include the use of electronic data capture systems, paper forms, or other means of data collection.
08
Specify adverse events and safety monitoring: Include information about adverse events that participants might experience, how they will be monitored, and the measures in place to ensure participant safety.
09
Follow guidelines and regulatory requirements: Ensure compliance with national guidelines and regulatory requirements specific to trials. This may involve providing details about ethical considerations, informed consent, and institutional review board approvals.
10
Review and double-check: Before submitting the filled-out national trials stores form, review all the information you have entered. Make sure everything is accurate, complete, and properly formatted.

Who needs national trials stores?

01
Researchers and investigators: National trials stores are primarily needed by researchers and investigators conducting clinical trials. These individuals require a systematic and centralized approach to collect, manage, and store trial data.
02
Ethical review boards and regulatory bodies: National trials stores provide a means for ethical review boards and regulatory bodies to review and monitor clinical trials. These stores ensure that necessary information is available for evaluation and compliance purposes.
03
Participants and their representatives: Participants and their representatives also benefit from national trials stores by having a centralized repository for relevant trial information. It allows them to access and review details about the trial they are involved in.
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