Parallel imports of pharmaceuticals are controversial because their welfare effects are generally ambiguous. First, there is a tension between two major public-policy objectives: innovation and development of new drugs, on the one hand, and short-run cost-containment

HPRA Guide to Parallel Imports of Human Medicines AUT-G0006-13 5/35 1 SCOPE This guide applies to nationally-authorised products which are parallel-imported from another EU Member State or another EEA country and distributed on the Irish market. In order to legally place such a product on the Irish market a parallel import licence is required

11 August 2017. List of parallel import licences granted in July 2017 This webinar gives an introduction to the European case-law on the parallel importation of pharmaceutical preparations and the principle of exhaustion of trade mark rights. Against this background, it will be discussed how this case law applies to other product categories such as foodstuffs and – most recently – medicinal products. IPLawIPREnforcement series course. Speaker: Dr. David.

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This is what makes them grey market goods. Parallel Imports and the Pricing of Pharmaceutical Products: Evidence from the European Union1 Mattias Ganslandt The Research Institute for Industrial Economics and Keith E. Maskus University of Colorado at Boulder Revision: February 2004 We consider policy issues regarding parallel imports (PIs) of brand-name pharmaceuticals in the Pharmaceutical imports into Turkey are regulated under the Pharmaceutical and Medical Preparations Law numbered 1262 (Law numbered 1262), while parallel imports and the exhaustion of rights principle are regulated by the Decree Law on the Protection of Trade marks numbered 556 (Trade mark Decree Law). Parallel trade in pharmaceuticals in Europe first appeared in the early 1970s, primarily in Germany, the Netherlands and the United Kingdom. Today these countries — along with Norway, Denmark and Sweden — continue to account for the highest proportion of parallel imports in the pharmaceutical market.

Parallel import of pharmaceuticals is when original medicine is imported from another EU/EEA country and sold in Denmark on par with the original manufacturer’s Danish packaging. We find that authorizing parallel imports can result in higher firm profit and/or social welfare than using ERP. We also examine, in a decentralized supply chain, two variations of ERP that are used in practice, the ex‐factory‐based ERP and the pharmacy purchase price (PPP)‐based ERP. pharmaceutical prices joined the EU, increased competition from parallel imports. Drugs facing competition from parallel imports are found to have on average 17% to 21% lower prices than they would have had if they had never faced such competition.

Under TRIPS, what are member governments' obligations on pharmaceutical In other words, even if a country allows parallel imports in a way that another 

In brief, parallel imports involve importing certain products, usually trademark-protected, through sales Parallel trade, the free movement of goods across Europe from lower-value to higher-value markets, has had a major impact on the European pharmaceutical industry since the 1970s. Parallel trade is viewed rather differently by pharmaceutical companies and parallel traders, and this made for some contrasting perspectives at the SMi Group’s 8th Parallel Trade conference, held in London in Parallel imports and the pricing of pharmaceutical products: evidence from the European Union. Ganslandt M(1), Maskus KE. Author information: (1)The Research Institute of Industrial Economics, P.O. Box 5501, SE-11485 Stockholm, Sweden. mattias.ganslandt@iui.se HPRA Guide to Parallel Imports of Human Medicines AUT-G0006-13 5/35 1 SCOPE This guide applies to nationally-authorised products which are parallel-imported from another EU Member State or another EEA country and distributed on the Irish market.

HPRA Guide to Parallel Imports of Human Medicines AUT-G0006-13 5/35 1 SCOPE This guide applies to nationally-authorised products which are parallel-imported from another EU Member State or another EEA country and distributed on the Irish market. In order to legally place such a product on the Irish market a parallel import licence is required

The UK parallel import licensing scheme lets a medicine authorised in European Economic Area (EEA) Member State be marketed in the UK, as long as the imported product has no therapeutic difference Many pharmaceutical manufacturers, however, are understandably concerned that parallel importation could lead to diminished profits, thereby reducing research and development efforts, and leading to a slowdown in the innovation of new drugs. Even worse, in certain situations, parallel imports could put the public health at risk. 2015-04-06 · Parallel imports of pharmaceuticals can put the public health at risk, as the quality of the drugs is not guaranteed. In theory, the Drug Administration of Vietnam (DAV), when weighing the decision to grant a parallel import license, will focus on the price and the name of the drugs, but not the quality.

No 852: Market  omregleringen leder dock inte parallellimport till signifikant lägre listpriser. of Parallel Imported Pharmaceuticals”, The B.E. Journal of Economic Analysis and  Supply Chain Manager Parallel Import. Teva Pharmaceuticals. Consultant, Supply Chain Management. self-emplyed. Production Planner. Så fungerar parallellimport av läkemedel.
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Yet, after first being put on the market, the goods are imported into an economic area and sold there without the consent of the trade mark owner. This is what makes them grey market goods.

Importers purchase goods that have already been placed on the market in the EEA and then import them into the UK to distribute and sell on to UK customers. A parallel import is a non- counterfeit product imported from another country without the permission of the intellectual property owner. Parallel imports are often referred to as grey product and are implicated in issues of international trade, and intellectual property. - The parallel-imported product must have the same active substance(s), the same pharmaceutical form and be identical to, or have no significant therapeutic difference from, the Irish-market product.
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Parallel imports from countries both outside and inside the European Economic Area (EEA) are to be found in a large number of trade sectors, such as clothing, footwear, capital goods, cars, pharmaceuticals, etc. In brief, parallel imports involve importing certain products, usually trademark-protected, through sales

Mar 6, 2019 Their January guide to what a “no-deal” Brexit means for medicines states clearly : “EU exit does not mean that parallel imports of medicines will  The UK parallel import licensing scheme lets a medicine authorised in European Economic Area ( EEA ) Member State be marketed in the UK, as long as the  This is partly due to parallel import of pharmaceuticals being more widespread in the primary care sector than in the hospital sector.

The book comprises thoughtful contributions on varying commercial aspects of IP, from parallel imports of pharmaceuticals to exhaustion of rights, and from trade 

The application form for a medicinal product imported in parallel refers to the valid marketing authorisation of the original product. Pharmaceutical imports into Turkey are regulated under the Pharmaceutical and Medical Preparations Law numbered 1262 (Law numbered 1262), while parallel imports and the exhaustion of rights principle are regulated by the Decree Law on the Protection of Trade marks numbered 556 (Trade mark Decree Law). Jul 5, 2016 The second defendant was a company that was set up to apply for and hold the product licences for parallel imports (PLPIs). Flynn Pharma holds  There have been proposals in the United States to permit parallel imports of pharmaceuticals from Canada (and other countries) in the last several years. The U.S.  According to the EFPIA, in 2006, parallel imports accounted for almost 15% of the UK import market, and the Association of the British Pharmaceutical Industry  Parallel trade of pharmaceuticals in the EU/EEA occur when pharmaceutical products are lawfully distributed in another Member State independently of the  However, US patent owners are protected from parallel imports in prescription drugs by an explicit right of importation. (As mentioned in the introduc- tion, this  There is trade in parallel imports in a wide range of goods, including such items as pianos, automobiles, motorcycles, chemicals, pharmaceuticals, computers,  Poget analyses how parallel imports of pharmaceuticals are affecting end consumer prices and drug expenditures in three Scandinavian countries, Sweden,  Keywords: parallel imports, manufacturer rebate, pharmaceuticals, regulation.

Insight from Life Science consultant and thought leader Global Pharma Consulting.