Global Certificate in Trial Participant Screening
-- ViewingNowThe Global Certificate in Trial Participant Screening is a comprehensive course designed to equip learners with the essential skills needed to excel in the field of clinical trials. This course highlights the importance of accurate participant screening, a critical component in clinical research that ensures the safety and efficacy of new treatments.
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• Eligibility Criteria for Clinical Trials: Understanding the basic criteria for selecting trial participants, including medical history, physical examination, and lab tests. • Informed Consent Process: Explaining the importance of informed consent, the elements of informed consent documents, and the process of obtaining consent from trial participants. • Screening Procedures: Describing the various screening procedures, such as medical history review, physical examination, and laboratory tests, used to determine trial eligibility. • Data Collection and Management: Discussing the importance of accurate and complete data collection and management during the screening process. • Privacy and Confidentiality: Explaining the legal and ethical requirements for protecting the privacy and confidentiality of trial participants' personal and medical information. • Regulatory Compliance: Outlining the regulatory requirements for trial participant screening, including Good Clinical Practice (GCP) guidelines and International Council for Harmonisation (ICH) standards. • Diversity and Inclusion: Discussing the importance of diversity and inclusion in clinical trials and strategies for recruiting and retaining a diverse trial participant population. • Ethical Considerations: Exploring the ethical considerations in trial participant screening, such as ensuring equitable access to clinical trials and minimizing potential harm to participants.
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- BasicUnderstandingSubject
- ProficiencyEnglish
- ComputerInternetAccess
- BasicComputerSkills
- DedicationCompleteCourse
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- ComplementaryFormalQualifications
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- ThreeFourHoursPerWeek
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