Answer: D. Annual Safety Report
Explanation:
The FDA requires that when there is a chance that an adverse effect might occur in a clinical trial, that it is included in certain documents.
It is to be included in an investigator brochure to ensure that the investigators are aware.
Protocol documents should also have the events disclosed and the the clinical participants should be aware of it in the Informed Consent Form that they sign.
An Annual Safety Report is not a primary source document in the first place so is the wrong option here.
Answer:
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Step by step explanation:
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Sharp and shooting Hope this helps!!
Tracheostomy is the opening created at the front of the neck where a pipe is being inserted for a patient to breath normally.
<h3>What is suctioning of tracheostomy?</h3>
The suctioning of tracheostomy is a nursing procedure that is being carried out by a Train band certified registered Nurse.
The process requires a careful step to prevent the patient from suffering from hypoxemia, which is decreased oxygen content of the blood.
In order to prevent hypoxemia during the suctioning procedure,
- Pause for 30 to 60 seconds between suctioning attempts.
- Limit suctioning to 10 to 15 seconds each time.
- Hyperventilate the client with 3 to 6 breaths before suctioning.
Learn more about hypoxemia here:
brainly.com/question/27960229
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