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Hide Image in the Clinical Trial Agreement

Hide Image in the Clinical Trial Agreement and eSign it in minutes

Aug 6th, 2022

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How to Hide Image in the Clinical Trial Agreement

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um Im excited today to kick off the fall clinical trials toolkit series um our first one is the office of sponsored programs clinical trial agreement review and negotiation um today we have Rachel humberson she is the interim assistant director um from research office and office of sponsored programs and we also have um Julie even though I practiced it Julie Im going to mess it up Anna okay is that right yeah okay she is a negotiator with research with the research office and office of sponsored programs um before I read their um their bios and a fun fact about them again we are offering continuing education to WVU employees so if um you would like CES please indicate that and please put your name um an email address in the chat so for attendance purposes um Im trying to think if theres anything else oh if you have a question during this um feel free to put it in the chat well be watching it and um I will stop Rachel and Julie and let them know what your question is and then also

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Got questions?

Below are some common questions from our customers that may provide you with the answer you're looking for. If you can't find an answer to your question, please don't hesitate to reach out to us.

What is the privacy rule in clinical trials?

The Privacy Rule is a response to public concern over potential abuses of the privacy of health information. The Privacy Rule establishes a category of health information, referred to as PHI, which may be used or disclosed to others only in certain circumstances or under certain conditions.

What is blinding or masking in a trial?

Blinding or masking (the process of keeping the study group assignment hidden after allocation) is commonly used to reduce the risk of bias in clinical trials with two or more study groups.

Why do we blind in clinical trials?

Blinding (sometimes called masking) is used to try to eliminate such bias. It is a tenet of randomised controlled trials that the treatment allocation for each patient is not revealed until the patient has irrevocably been entered into the trial, to avoid selection bias.

How do you anonymize clinical trial data?

This allows for meaningful secondary analyses and follow-on research while maintaining patient confidentiality. Examples of anonymization include redacting the name, date of birth and other demographic identifiers of individuals associated with the conduct of the trial.

What does blinded mean in clinical research?

(BLINE-ded STUH-dee) A type of study in which the patients (single-blinded) or the patients and their doctors (double-blinded) do not know which drug or treatment is being given.

What are the advantages of blindness in clinical trials?

The blinded trial approach has been shown to provide a more complete understanding of a drugs effectiveness, benefits, and the range of possible adverse reactions without the bias of the placebo effect.

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