The FDA Law Blog

MAY 13, 2024

FDA believes that RWE has the power to “accelerate medical product development and bring new innovations and advances faster and more efficiently to the patients who need them, without compromising patient safety.” This guidance, when finalized, will replace the original version of this document finalized in 2017.

FDA 109

FDA Medical Records Documentation 109

Hospital Pharmacy Europe

AUGUST 7, 2024

The incidence of medication errors varies greatly among published studies, not only due to the lack of a clear definition, 1,2 but also because of different factors such as the healthcare setting, differing levels of automation (e.g. 3–5 Medication errors are often documented in national or local electronic incident reporting systems.

Hospitals 98

Hospitals Documentation Medical Records Dosage 98

Pharmaceutical Technology

JUNE 20, 2023

GlobalData forecasts that the market for AI platforms for the entire healthcare industry will reach $4.3bn by 2024, up from $1.5bn in 2019 [i]. Consent documents often describe technical medical conditions and regulatory bodies are increasing pressure on sponsors to ensure that patient-facing information can be easily understood by patients.

Medical Records 52

Medical Records Documentation Communication Dosage 52