- Informed consent: what’s allowed and what’s practical in obtaining consent remotely, where does electronic consent come in, and whether participant compensation needs to be modified
- How do IRBs consider the review of “virtual” clinical trials?
- What do sponsors consider when deciding whether study visits can be conducted remotely, both when planning ahead, and when reacting to urgent issues?
Most Recent Flipbooks
16 industry experts share shifts and trends that will inform clinical research in 2020 and beyond.
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Something Has to Give: The Current Unsustainable Approach to Safety Reporting Puts Trials and Patients at Risk