Medical Research

Updated Common Rule Regulations for Medical Research in the 21st Century

Updated Common Rule Regulations for Medical Research in the 21st Century

By

The 2017 revisions to the Common Rule deal largely with improving the transparency and clarity of intended uses under the current standard of informed consent while introducing a new concept of "broad consent".

Reporting Negative Data in Clinical Trial Results

Reporting Negative Data in Clinical Trial Results

By

Increasingly, the scientific community is coming to realize the invaluable role that negative outcomes play in the understanding of medicine as a whole.

Informed Consent in Medical Research: A Q&A

Informed Consent in Medical Research: A Q&A

By

New methods of obtaining consent are offering options that can bridge the geographic distances between researcher and participant, while making study information more easily accessible.

Sign Up for Free e-Newsletters