Medical Devices: Classification and Analysis of Faults Leading to Harms

Author:

Ferner Robin E.ORCID,Aronson Jeffrey K.ORCID

Publisher

Springer Science and Business Media LLC

Subject

Pharmacology (medical),Pharmacology,Toxicology

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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