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[Show more]Phase I Trial AKA - ANSWER Human Pharmacology 
 
Phase I Trial - ANSWER -Assess tolerance. 
-Define/describe PK and PD. 
-Explore drug metabolism and drug interactions, estimate activity. 
-Done in healthy volunteers.10 -100 people 
 
Phase II Trial AKA - ANSWER Therapeutic Exploratory ...
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Add to cartPhase I Trial AKA - ANSWER Human Pharmacology 
 
Phase I Trial - ANSWER -Assess tolerance. 
-Define/describe PK and PD. 
-Explore drug metabolism and drug interactions, estimate activity. 
-Done in healthy volunteers.10 -100 people 
 
Phase II Trial AKA - ANSWER Therapeutic Exploratory ...
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A subject in an arthritis clinical trial develops a severe cold and flu like symptoms. This event is most likely classified as a) An adverse event 
b)	An adverse drug reaction 
c)	An unexpected adverse drug reaction 
d)	A serious adverse event 
 
b)	A causal relationship between drug and advers...
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Add to cartA subject in an arthritis clinical trial develops a severe cold and flu like symptoms. This event is most likely classified as a) An adverse event 
b)	An adverse drug reaction 
c)	An unexpected adverse drug reaction 
d)	A serious adverse event 
 
b)	A causal relationship between drug and advers...
The _________ has developed the Declaration of Helsinki (DoH): - ANSWER World 
Medical Association; as a statement of ethical principles to provide guidance to 	 
physicians and other participats in medical research involving human subjects.	 
 
(DoH) It is the duty of ________________ in medica...
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Add to cartThe _________ has developed the Declaration of Helsinki (DoH): - ANSWER World 
Medical Association; as a statement of ethical principles to provide guidance to 	 
physicians and other participats in medical research involving human subjects.	 
 
(DoH) It is the duty of ________________ in medica...
What are expected or possible consequences of over-estimation of recruitment 
potential? - ANSWER - The trial will overrun its projected timeline - The recruitment period will be prolonged and more sites may be needed - The study will not have sufficient data within the required timeframe and will...
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Add to cartWhat are expected or possible consequences of over-estimation of recruitment 
potential? - ANSWER - The trial will overrun its projected timeline - The recruitment period will be prolonged and more sites may be needed - The study will not have sufficient data within the required timeframe and will...
What statements are true concerning an adverse drug reaction? - ANSWERS - All noxious and unintended responses to a medicinal product related to any dose should be considered as an ADR 
-	An ADR suggests a relationship to trail medication 
-	All ADRs must be documented 
 
What Adverse Events (AE...
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Add to cartWhat statements are true concerning an adverse drug reaction? - ANSWERS - All noxious and unintended responses to a medicinal product related to any dose should be considered as an ADR 
-	An ADR suggests a relationship to trail medication 
-	All ADRs must be documented 
 
What Adverse Events (AE...
Approval (in relation to Institutional Review Boards) - ANSWER The affirmative decision of the IRB that the clinical trial has been reviewed and may be conducted at the institution site within the constraints set forth by the IRB, the institution, Good Clinical Practice (GCP), and the applicable re...
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Add to cartApproval (in relation to Institutional Review Boards) - ANSWER The affirmative decision of the IRB that the clinical trial has been reviewed and may be conducted at the institution site within the constraints set forth by the IRB, the institution, Good Clinical Practice (GCP), and the applicable re...
1571 - ANSWER IND application; Permit to do research on humans for the first time; 
has background info; and rationale; updated annually	 
 
1572 - ANSWER Investigator statement; commitment, done nationally and 
internationally by sponsors intending to hava marketing aproval for IP	 
 
IB - ...
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Add to cart1571 - ANSWER IND application; Permit to do research on humans for the first time; 
has background info; and rationale; updated annually	 
 
1572 - ANSWER Investigator statement; commitment, done nationally and 
internationally by sponsors intending to hava marketing aproval for IP	 
 
IB - ...
Belmont Report (1979) - ANSWER ethical principles and guidelines for the protection of 
human subjects of research.	 
 
respect for persons - ANSWER individuals should be treated as autonomous agents 
and persons with diminished autonomy are entitled to protection	 
 
An autonomous person - ...
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Add to cartBelmont Report (1979) - ANSWER ethical principles and guidelines for the protection of 
human subjects of research.	 
 
respect for persons - ANSWER individuals should be treated as autonomous agents 
and persons with diminished autonomy are entitled to protection	 
 
An autonomous person - ...
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