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Informed consent is the process of learning about a clinical research trial
you can choose to stop participating in the trial at any time
clearly understand the information about a trial
the possible risks and benefits of participating
If you have someone who can legally make health decisions for you
What is eConsent?
Providing your signature in the eConsent
eConsent should be easy to understand
Intro
Why are we looking at these use cases in combination?
Informed Consent
Patient Enrolment
Patient app demonstration
How PharmaLedger is being validated with patients and investigators
Factors involved in delivery of patient-centric clinical trials
Does the eConsent solution fulfill legal requirements?
Do patients have the option to download all or part of their data?
Closing Remarks
求める情報が見つからない場合は、キーワードや指定した条件を変えてみてください。