Results 81 to 90 of about 352,837 (117)
The Impact of Serialisation on Operational Efficiency and Productivity in Irish Pharmaceutical Sites. [PDF]
O' Mahony D, Lynch A, McDermott O.
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Ritual to relief: ethical frontiers in repurposing psychoactive substances. [PDF]
O'Leary E, Dodd S, Stahl S.
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Actor-network and stakeholder analysis in preventing health goods smuggling in Iran. [PDF]
Meymand FM, Takian A, Jaafaripooyan E.
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Policy options for sustainable access to off-patent antibiotics in Europe. [PDF]
Panteli D +7 more
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Antibiotic surveillance: an action-oriented integrated approach. [PDF]
Valsson O +41 more
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Approval delays in multi-country COVID-19 trials: the case of COPCOV and the risk of therapeutic inertia. [PDF]
Winters J, Schilling WH.
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European Union has the Falsified Medicines Directive
BMJ, The, 2012Attaran and colleagues made no mention of a current important European Union directive: the so called Falsified Medicines Directive.1 …
exaly +3 more sources
Substandard and Falsified Medicines in Myanmar
Background: substandard and falsified medicines (SFMs) are a threat to public health. The availability of SFMs in Myanmar was reported by the World Health Organization (WHO) in 1999, but there have been few systematic surveys on falsified medicines in ...
Naoko Yoshida +2 more
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Pharmaceutical Medicine, 2019
Regulatory capture describes the phenomenon in which regulators (e.g. medical agencies) protect the interest of the companies they regulate rather than the interest of the public. Not much is known about the mechanisms of this potential threat within the area of pharmaceutical regulation.Through a comparison of two EU member states, the Netherlands and
Rasmus Borup +2 more
openaire +3 more sources
Regulatory capture describes the phenomenon in which regulators (e.g. medical agencies) protect the interest of the companies they regulate rather than the interest of the public. Not much is known about the mechanisms of this potential threat within the area of pharmaceutical regulation.Through a comparison of two EU member states, the Netherlands and
Rasmus Borup +2 more
openaire +3 more sources
The EU Falsified Medicines Directive - A Concept for Drug Decommissioning in Hospitals.
Studies in health technology and informatics, 2019The 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.
Sandra, Burri, Rebecca, Scheidegger
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