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20172018 CLINICAL
INSTRUCTOR
Handbooks
A guide to clinical instruction as set forth by the Laramie County Community
College Diagnostic Medical Sonography Program and by the JRC DMS and
CACHE accrediting
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Step 1: Read and understand the purpose of the guide to clinical.
02
Step 2: Familiarize yourself with the required sections and information that need to be included in the guide.
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Step 3: Gather all the necessary documents and materials related to the clinical process.
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Step 4: Start by providing general information about the clinical, such as the title, date, and location.
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Step 5: Clearly outline the objectives and goals of the clinical.
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Step 6: Describe the methodology and procedures that will be followed during the clinical.
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Step 7: Present any ethical considerations or approvals that were obtained for the clinical.
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Step 8: Provide a detailed timeline or schedule for the clinical activities.
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Step 9: Include any necessary forms, templates, or consent documents that participants need to fill out.
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Step 10: Conclude the guide by summarizing key points and providing contact information for further inquiries.
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Step 11: Proofread and edit the guide to ensure clarity and accuracy.
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Step 12: Distribute the guide to all relevant parties involved in the clinical.
Who needs a guide to clinical?
01
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Participants in the clinical trial
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Ethics committees or review boards overseeing the clinical
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What is a guide to clinical?
A guide to clinical is a document that outlines the procedures and protocols for conducting clinical trials.
Who is required to file a guide to clinical?
Researchers and organizations conducting clinical trials are required to file a guide to clinical.
How to fill out a guide to clinical?
A guide to clinical can be filled out by providing detailed information on the study objectives, methodology, participant criteria, and data analysis plan.
What is the purpose of a guide to clinical?
The purpose of a guide to clinical is to ensure transparency and consistency in the conduct of clinical trials.
What information must be reported on a guide to clinical?
Information such as study protocol, informed consent forms, study design, statistical analysis plan, and adverse event reporting procedures must be reported on a guide to clinical.
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