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Clinical Research Basics ClinicalTrrialsLaborato ORY, LaboratorryServices(TTL)withinAlbbertaHealthServicesandtheNorthern n AlbertaCllinicalTrialsaandResearchCentre(ACTOR)arepleaasedtopresentClinicalResearchBasicss.
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Review the study protocol and familiarize yourself with the inclusion and exclusion criteria.
02
Obtain informed consent from participants before enrolling them in the study.
03
Collect relevant data and information according to the study protocol.
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Monitor participants throughout the study and record any adverse events or outcomes.
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Analyze the data collected and draw conclusions based on the results.
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Prepare a written report summarizing the findings and submit it for publication or presentation.

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Clinical researchers, scientists, physicians, and other healthcare professionals who are conducting or participating in clinical trials or research studies.
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Clinical research is a type of study that involves testing new medical treatments or interventions on human subjects to determine their safety and effectiveness.
Researchers, institutions, and sponsors involved in clinical research are required to file the necessary paperwork with regulatory authorities.
Clinical research forms must be filled out accurately and completely, following the guidelines provided by regulatory authorities.
The purpose of clinical research is to gather data on new medical treatments or interventions to determine their safety and efficacy before they are approved for widespread use.
Clinical research forms typically require information on the study protocol, research team, potential risks and benefits, and data collection methods.
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