Förlagets beskrivning
Informed consent and institutional review boards in clinical trials. For beginner to advanced- for pharmaceutical and medical device companies, CROs, FDA-regulated industries, and all workers in medical studies that follow good clinical practices for the protection of human subjects in experimentation. Also relevant to biomedical ethics
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Agent GCP and the Bloody Consent Form, 10 Users
Bokrecensioner » Agent GCP and the Bloody Consent Form, 10 Users
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