Easily Hide Date Field from the Clinical Trial Agreement

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How to Hide Date Field from the Clinical Trial Agreement

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hey everyone its dance fair from the clinical trials guru back with yet another video every day I try to do more than one a day but today Im doing this one its a pretty special video somewhat important as I tell you guys all the time you especially you research clinics but this doesnt just apply for to research clinics it applies to everybody in this industry whether you work for a CRO whether youre a p.i wanting to network with other p is whether your site director of a research clinic even sponsors its so important in this industry to network with your colleagues even if its from competing companies even the Big Pharma is doing this now youre seeing a lot of collaboration going on between Big Pharma so theres no reason as research sites should not be able to do this so Im part of of several groups on LinkedIn there are some Google Plus groups theres my special cyber dusters for those of you who dont know cyber dust is an app you can add me dance vera im planning to start

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What is considered source data for a clinical trial?

What is source data? The executive order on GCP defines source data as any information in original records and certified copies of original records of clinical findings, observations or other activities in a clinical trial necessary for the reconstruction and evaluation of the trial.

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.

How do you write a date in clinical research?

Following ISO 8601 standards, CDISC takes YYYY-MM-DD as its date format.

Can date of birth be collected in clinical trials?

Examples of patient-level data collected in clinical trials are patient identifier, site identifier, date of birth, gender, race, efficacy outcomes, laboratory test results, etc.

What are subject identifiers in clinical trials?

Per federal human subjects regulations, any information that renders a person readily identifiable is a subject identifier. Under HIPAA regulations about Protected Health Information, 18 specific information elements (e.g., name, medical record number, birth date) are always considered to be subject identifiers.

What data is collected during clinical trials?

Data collection for clinical research involves gathering variables relevant to research hypotheses. These variables (patient parameters, data items, data elements, or questions) are aggregated into data-collection forms (Case Report Forms or CRFs) for study implementation.

How do you write dates in clinical research?

Following ISO 8601 standards, CDISC takes YYYY-MM-DD as its date format.

What excludes you from clinical trials?

What is exclusion criteria? Exclusion criteria is a list of characteristics that disqualify a person from participating in a clinical trial. These characteristics can vary from demographic information like age, gender, or race to something as complex as comorbidities, organ dysfunction, or the use of other medications.

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Hide Date Field from the Clinical Trial Agreement