Medical Devices: Classification and Analysis of Faults Leading to Harms
Author:
Publisher
Springer Science and Business Media LLC
Subject
Pharmacology (medical),Pharmacology,Toxicology
Link
http://link.springer.com/content/pdf/10.1007/s40264-019-00879-2.pdf
Reference41 articles.
1. Aronson JK, Heneghan C, Ferner RE. Medical devices: definition, classification, and regulatory implications. Drug Saf. 2019. https://doi.org/10.1007/s40264-019-00878-3 .
2. Ferner RE, Aronson JK. Medication errors, worse than a crime. Lancet. 2000;355(9208):947–8.
3. European Medicines Agency. Medication errors. https://www.ema.europa.eu/en/human-regulatory/post-authorisation/pharmacovigilance/medication-errors . Accessed 25 Oct 2019.
4. Aronson JK, Ferner RE. Clarification of terminology in drug safety. Drug Saf. 2005;28(10):851–70.
5. Medicines and Healthcare products Regulatory Agency (MHRA). Alerts and recalls for drugs and medical devices. https://www.gov.uk/drug-device-alerts . Accessed 25 Oct 2019.
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