The FDA updated their Mobile Medical Application guidance on May 29, 2018. Learn more here: https://www.fda.gov/medicaldevices/digitalhealth/mobileme... (continued)
Describes how to conduct reseach using digital technology and what considerations to be conscious of when conducting this research.
The draft guidance provides recommendations to sponsors, clinical investigators, IRBs, CROs, and other interested parties on the use of electronic rec... (continued)
The Department of Health and Human Services Office of Civil Rights (OCR) recently released guidance on HIPAA and cloud computing that clarifies that C... (continued)
This document is a set of best practices for researchers—especially junior researchers—who wish to engage in research that may make the researcher sus... (continued)
The FDA released this guidance on Adaptive Designs for medical devices in clinical trials. An adaptive design for a medical device clinical study is d... (continued)
Participant Population: IRB Professionals Study Type: Exempt Field: Public Health Description: Using private messaging on LinkedIn to recruit particip... (continued)
If you are engaging in research in the state of California, there are California Laws that dictate over PII, Privacy, Student Records, Medical Applic... (continued)