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Supplemental Materials Challenges of conducting clinical trials during the SARSCoV2 pandemic: The ASCEND global program experience Kirsten L. Johansen, Anjali Zachary, Bout Cayman, Alexander R. Cubits,
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How to fill out challenges of conducting clinical

01
Identify the specific objectives of the clinical study.
02
Prepare a detailed study protocol outlining the study design, procedures, and criteria for participation.
03
Obtain ethical approval from the relevant research ethics committee.
04
Recruit suitable participants for the study and obtain informed consent.
05
Implement the study according to the protocol and collect data.
06
Analyze the data and draw conclusions based on the results obtained.

Who needs challenges of conducting clinical?

01
Researchers conducting clinical studies.
02
Healthcare professionals looking to improve patient care through evidence-based practices.
03
Drug companies seeking to test the safety and efficacy of new medications.
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Regulatory bodies responsible for approving new medical treatments.
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The challenges of conducting clinical trials include recruitment of participants, regulatory hurdles, data collection and analysis, and ensuring the safety and ethical treatment of participants.
Researchers, sponsors, and clinical trial staff are required to report challenges of conducting clinical trials.
Challenges of conducting clinical trials can be filled out by documenting any difficulties or obstacles faced during the trial process.
The purpose of challenges of conducting clinical trials is to ensure transparency and accountability in the research process.
Information such as recruitment difficulties, protocol deviations, adverse events, and delays in data collection must be reported on challenges of conducting clinical trials.
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