sickfees.ie
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HPRA still require local approval, this is largely about the outer packaging and the insert leaflet.My local pharmacist told me that many drugs which are available elsewhere in the EU are not available in Ireland as it's not worth their while applying for an Irish license. I was surprised at this as I had assumed if the EU had approved it, we should not add another layer of approval.
Brendan
The Irish market is relatively so small that many suppliers won't bother.
As my daughter says the juice is not worth the squeeze!
Under EU law any EU approved prescribed human product can be imported by a registered importer.
Anyone can register as an importer. Obviously an applicant would have to show the HPRA that have the required expertise and facility to control prescribed medication.
"Where the product to be imported differs in any respect from that on the Irish market, a parallel import licence (termed a ‘parallel product authorisation’) must be obtained; Where the product to be imported is identical in all respects (including identical packaging, labels and leaflets) to the product on the Irish market, a parallel import licence (termed a Dual Pack import Registration (DPR)) is required; "