The Falsified Medicines Directive is a legal framework introduced by the European Commission, to improve the protection of public health within the European Union. The directive applies since 2 January 2013. The European Commission Delegated Regulation, (EU) 2016/161, supplements Directive 2001/83/EC with rules regarding safety features for the packaging of medicinal products for human use. The regulation was adopted in October 2015. Measures to counteract to fake medicines include stricter record-keeping of wholesale distributors, tougher inspections of pharmaceutical producers, an EU-wide quality mark to identify online pharmacies and obligatory safety features on packages.
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| - Directiva 2011/62/UE (es)
- Falsified Medicines Directive (en)
- Конвенція про підроблення медичної продукції (uk)
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| - Конвенція про підроблення медичної продукції (англ. Falsified Medicines Directive) — серія постанов Європейської комісії, що мають на меті протистояння розповсюдженню підроблених лікарських засобів на території Європейського Союзу. (uk)
- The Falsified Medicines Directive is a legal framework introduced by the European Commission, to improve the protection of public health within the European Union. The directive applies since 2 January 2013. The European Commission Delegated Regulation, (EU) 2016/161, supplements Directive 2001/83/EC with rules regarding safety features for the packaging of medicinal products for human use. The regulation was adopted in October 2015. Measures to counteract to fake medicines include stricter record-keeping of wholesale distributors, tougher inspections of pharmaceutical producers, an EU-wide quality mark to identify online pharmacies and obligatory safety features on packages. (en)
- Conocida como la "Directiva de medicamentos falsificados", fue creada para combatir la amenaza del incremento de dichos medicamentos en la Unión Europea. Se trata de una Directiva del Parlamento Europeo y del Consejo de la Unión Europea, redactada en Estrasburgo, que modifica la anterior de 2001/83/CE (Directiva 2001/83/CE) que ya fue modificada en 2010 por la Directiva 2010/84/UEen lo relativo a la Farmacovigilancia. (es)
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| - Conocida como la "Directiva de medicamentos falsificados", fue creada para combatir la amenaza del incremento de dichos medicamentos en la Unión Europea. Se trata de una Directiva del Parlamento Europeo y del Consejo de la Unión Europea, redactada en Estrasburgo, que modifica la anterior de 2001/83/CE (Directiva 2001/83/CE) que ya fue modificada en 2010 por la Directiva 2010/84/UEen lo relativo a la Farmacovigilancia. Esta nueva modificación, además de introducir el establecimiento y regulación de un código comunitario en relación con los medicamentos de uso humano, incluye una serie requerimientos técnicos que serán aplicados en la fabricación y distribución de medicamentos y principios activos La propuesta de esta Directiva fue redactada por la Comisión Europea y aprobada en junio de 2011. Posteriormente se publicó en el Diario Oficial de la Unión Europea el 1/7/2001 y entró en vigor 20 días después de dicha publicación. (es)
- The Falsified Medicines Directive is a legal framework introduced by the European Commission, to improve the protection of public health within the European Union. The directive applies since 2 January 2013. The European Commission Delegated Regulation, (EU) 2016/161, supplements Directive 2001/83/EC with rules regarding safety features for the packaging of medicinal products for human use. The regulation was adopted in October 2015. Measures to counteract to fake medicines include stricter record-keeping of wholesale distributors, tougher inspections of pharmaceutical producers, an EU-wide quality mark to identify online pharmacies and obligatory safety features on packages. It requires that a unique identifier must be encoded in a two-dimensional barcode printed on each unit of sale package which is to contain:
* Product code
* Randomized serial number
* Expiration date
* Batch or lot number
* National Health Reimbursement Number if required There must be a Tamper Evident Device. When the medicine or vaccine is dispensed it must be scanned and the barcode decommissioned, so that it cannot be reused on a falsified medicine. 2,291 pharmaceutical companies with marketing authorisations to supply prescription medicines to the European Economic Area are required to connect to the EU Hub established by the European Medicines Verification Organisation and upload the unique identifier for each pack of medicine they manufacture or repackage before February 2019. By August 2018 only 841 companies had completed the first stage of connection, which may take up to six months. The Market Pharmacy in Bolton, which is part of the Hollowood Chemists group claimed in December 2018 to be the first compliant pharmacy in the UK when it connected to the UK in December 2018. The directive ceased to apply in Great Britain, except in Northern Ireland, at the end of the Brexit transition period. (en)
- Конвенція про підроблення медичної продукції (англ. Falsified Medicines Directive) — серія постанов Європейської комісії, що мають на меті протистояння розповсюдженню підроблених лікарських засобів на території Європейського Союзу. (uk)
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