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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
a wholesaler’s
Guide to Registration Requirements for Brokers of Medicinal Products in Ireland
Guide to Registration Requirements for Brokers of Medicinal Products in Ireland,
AUT-G0106-2 1/4
Guide to
Registration Requirements for Brokers of
Medicinal Products in Ireland
1
INTRODUCTION
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.
The FMD defines, products identified as falsified or suspected to be falsified.
HPRA Guide to Registration
Information for Brokers
? The term 'broker' as introduced by the Falsified Medicines Directive, refers to a person, the Falsified Medicines Directive bring for my company? A broker must comply with the requirements, & 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
Strategic Plan 2016 - 2020 Consultation Response Document
to continue to focus on falsified medicines, illegal internet sales and supply chain activities, the regulation of medicines, medical devices and other health
products. In carrying out our, related to the regulation of human medicines. A number of
concerns were raised by more than one respondent, especially concerning the area of access to
medicines. Medicines shortages which have, for their
patients.
Another priority for some respondents was the reclassification of medicines from
Applications for a Wholesale Distribution Authorisation
on the Irish Market Controlled Drugs Falsified Medicines Legislation Parallel, , 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 2 January 2013, , Authority, HPRA, Ireland, Eire, European Union, Safety & Quality, Medicines, Medical Devices, Blood, , the quality, safety and efficacy of medicines available in Ireland and to participate in systems designed
Batch-Specific Requests for Human Medicines
) to be supplied. Highlight the differences.
Is the product compliant with the Falsified Medicines, Batch-Specific Requests for Human Medicines, Batch-specific Requests
For details of the requirements, please see the Guide to Batch-Specific Requests for Human Medicines. If the request refers to multiple MAs, refer to specific MAs throughout where appropriate.
Name and address of MA holder(s):
FORMTEXT
Direct telephone number: FORMTEXT
Email: FORMTEXT
Name
Dangers of buying prescription medicines online
through the internet). Manufacturing fake or counterfeit medicines – known as falsified medicines, Dangers of buying prescription medicines online,
HPRA Website, My HPRA Logout Dangers of buying prescription medicines online Buying prescription medicines on the internet might seem like a good idea but there is no way of knowing how safe these medicines are or if they will work properly. At best, you could simply