Results 91 to 100 of about 352,837 (117)
Some of the next articles are maybe not open access.

Implementation of the Falsified Medicines Directive in the secondary care environment - experiences and recommendations from European hospitals

Asian Journal of Biomedical and Pharmaceutical Sciences, 2021
The World Health Organisation estimates that up to 50% of medicinal products in the world are counterfeit. Counterfeit drugs pose a huge threat to human health and life. Although the number of counterfeit drugs in Europe is much lower than in developing countries, the European Union has developed a directive that prevents the trade in falsified drugs ...
Religioni, Urszula, Merks, Piotr
openaire   +1 more source

The EU Falsified Medicines Directive – A Concept for Drug Decommissioning in Hospitals

2019
The EU falsified Medicines Directive 2011/62/EU will be applied in Switzerland as well. It mandates unique identifiers on medication packages and a process to ensure that these identifiers are decommissioned when the medication package is handed to the patient.
Burri Sandra, Scheidegger Rebecca
openaire   +1 more source

New details emerge about the implementation of the Falsified Medicines Directive's safety features and verification requirements

European Journal of Hospital Pharmacy, 2015
All hospital pharmacies in Europe will be under a legal obligation to implement new medicines verification requirements in 2018. The new requirements come as a result of the 2011 Falsified Medicines Directive. Further details of what this is likely to mean in practice for hospital pharmacists have recently been emerging.
openaire   +1 more source

Current challenges in the detection and analysis of falsified medicines

Journal of Pharmaceutical and Biomedical Analysis, 2021
Bastiaan Venhuis   +1 more
exaly  

Home - About - Disclaimer - Privacy