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2/3/2015Data Management & Case Report Form Development in Clinical Trials Introduction to the Principles and Practice of Clinical Research February 3, 2015Marge Good, RN, MPH, OCN Nurse Consultant
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Step 1: Gather all necessary documents and materials for the clinical research.
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Step 2: Review the research protocol and understand the objectives and requirements.
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Step 3: Fill out the necessary forms and questionnaires accurately and thoroughly.
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Step 4: Collect and document any relevant data or measurements as specified in the protocol.
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Step 5: Submit the completed forms and data to the designated research coordinator or organization.
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Step 6: Follow any additional instructions or guidelines provided for the completion of the clinical research process.

Who needs of clinical research?

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Pharmaceutical companies conducting drug trials
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Medical research institutions and universities
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Healthcare organizations and hospitals
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Government agencies involved in public health initiatives
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Medical professionals looking to improve patient care and treatment options
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Patients and volunteers who are willing to participate in clinical trials
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Clinical research involves conducting studies on humans to evaluate the safety and effectiveness of new drugs, treatments, or medical devices.
Researchers, pharmaceutical companies, and medical institutions are required to file for clinical research.
Clinical research forms can typically be filled out online or through paper forms provided by the regulatory authorities.
The purpose of clinical research is to gather data to determine the safety and efficacy of new medical interventions.
Clinical research reports must include details of the study design, results, adverse events, and conclusions.
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