Informed consent: Maximising compliance and minimising risk
While the principle of participant consent is better appreciated in clinical research today than in previous decades, the opportunities for error remain...
Source: labnews.co.uk
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FDA Consolidates, Revises Informed Consent Guidance; 2018 Common Rule Not Addressed | Health Care Compliance Association (HCCA)
Nearly nine years to the day the Food and Drug Administration (FDA) issued a draft “information sheet” on informed consent, the agency published a 66-page final guidance document on the...
Source: jdsupra.com
FDA Publishes Informed Consent Final Guidance for Drug and Medical Device Clinical Investigations | Nelson Mullins Riley & Scarborough LLP
The U.S. Food and Drug Administration (FDA or the Agency) has issued the final guidance document, “Informed Consent: Guidance for Institutional Review Boards, Clinical Investigators,...
Source: jdsupra.com
Five Key Considerations for Study Pre-Screening and Recruitment Initiatives in the Digital Age | McDermott Will & Emery
Key players across the healthcare industry—including sponsors, contract research organizations (CROs), research sites, regulators and patient advocates—are well aware of the challenges...
Source: jdsupra.com
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The world's fascination with doppelgangers: Why are we so obsessed?
Now, there’s interest in using lookalikes for medical diagnosis and crime-solving.
Source: nzherald.co.nz