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D5.2 Capacity Building and Assessment Handbook for site readiness 853966 EUPEARL: EU PatientcEntric clinicAl tRial pLatforms WP5 Integrated Research Platform for Tuberculosis (TB)Lead contributorRiccardo
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Gather all necessary patient information including personal details (name, age, contact information).
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Review the trial protocol to understand the specific requirements for participation.
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Begin filling out the form by entering the patient's demographics in the designated sections.
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Provide medical history, including previous treatments and current medications.
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Clearly outline any allergies or adverse reactions to medications.
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Include information about the patient's consent for participation in the trial.
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Submit the completed form to the appropriate clinical trial coordinator or institution.

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Patients who wish to participate in clinical trials focused on patient-centric approaches.
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Clinicians and healthcare providers looking to enroll their patients in relevant clinical studies.
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Research organizations conducting patient-centric clinical trials.
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The EU Patient-Centric Clinical Trial form is a regulatory document designed to ensure that clinical trials within the European Union prioritize the needs and perspectives of patients throughout the research process.
Sponsors and researchers conducting clinical trials involving human participants in the EU are required to file the EU Patient-Centric Clinical Trial form.
To fill out the form, submitters need to provide comprehensive information about the trial's objectives, design, patient involvement strategy, and methods for patient engagement throughout the study.
The purpose of the form is to enhance the involvement of patients in clinical research, ensuring their feedback and experiences are integrated into trial protocols to improve relevance and outcomes.
The form must report information such as trial objectives, methodology, patient inclusion criteria, recruitment strategies, and how patient feedback will be collected and utilized.
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