Displaying 1 - 10 of 30 results.
Falsified Medicines Legislation
Falsified Medicines Legislation,
HPRA Website, My HPRA Logout Falsified Medicines Legislation
The European Union (EU) Falsified, the pharmaceutical supply chain from infiltration by falsified (or counterfeit) medicines and introduces new rules to more rigorously regulate the supply chain. The main provisions of the Falsified Medicines, .
The falsified medicines legislative proposal was adopted by the Council and European Parliament in June
HPRA - Press Release - Operation Pangea 2015
ONLINE FALSIFIED MEDICINES
Over 142,000 units of illegal prescription medicines, sale of
falsified (counterfeit and illegal) medicines where the HPRA, Revenue’s Customs Service, as the Falsified Medicines Directive – Directive
2011/62/EU) that came into force in Ireland in 2013.
networks behind the sale of counterfeit and illegal medicines via illicit online sales.
Locally, (analgesics), weight loss products as well as anabolic steroids and medicines indicated
(Epilim) Biosimilar Medicines Legal Classification / Method of Sale and Supply Falsified Medicines Legislation HPV School Immunisation Combined Hormonal Contraceptives, , Safety & Quality, Medicines, Medical Devices, Blood, Tissues & Cells, Cosmetics, Publications, with current medical and scientific knowledge, the quality, safety and efficacy of medicines available
Active Substance Registrations
for companies as required by Directive 2011/62/EU (Falsified Medicines Directive), began on the 2 January 2013, & Quality, Medicines, Medical Devices, Blood, Tissues & Cells, Cosmetics, Publications The objective, medical and scientific knowledge, the quality, safety and efficacy of medicines available in Ireland
HPRA - Press Release - 2014 Annual Report - 2Sept2015
Regulatory Authority Publishes
2014 Annual Report
More than 730,000 falsified medicines detained, of
falsified and illegal prescription medicines as well as on drawing attention to the associated
dangers. The list of interchangeable medicines, which facilitates generic substitution, s efforts during 2014 to stem the flow of falsified
medicines into Ireland and the concerns,
of prescription only medicines without prescription and wholesale of medicines without
Guide to Registration Requirements for Brokers of Medicinal Products in Ireland
Guide to Registration Requirements for Brokers of Medicinal Products in Ireland,
Registration Requirements for Brokers of
Medicinal Products in Ireland
Directive 2011/62/EU, known as the Falsified Medicines Directive (FMD), was published, at
preventing the entry of falsified medicines into the legal supply chain. Certain aspects, as falsified or suspected to be falsified.
HPRA Guide to Registration Requirements for Brokers of Medicinal
Information for Brokers
'broker' as introduced by the Falsified Medicines Directive, refers to a person or company, the Falsified Medicines Directive bring for my company?
A broker must comply with the requirements, , European Union, Safety & Quality, Medicines, Medical Devices, Blood, Tissues & Cells, Cosmetics, of medicines available in Ireland and to participate in systems designed to do that throughout