Πηγή: Independent
Pharmaceutical
companies spend tens of millions of euros on lobbyists every year to ensure
“privileged access” to decision-makers in Brussels, according to a major new
report that lifts the lid on their influence on EU drugs and healthcare policy.
The
industry now spends at least €40m annually – 15 times more than NGOs and
consumer groups, according to estimates – as representatives from “big pharma”
enjoy a “staggering” number of meetings with European Commission departments
and officials.
The
report published today by research and campaign group Corporate Europe
Observatory (CEO) reveals:
- The influential European Federation of Pharmaceutical Industries and Associations (Efpia) had over 50 meetings with the EU’s executive body during Jean-Claude Juncker’s first four and a half months as head of the Commission.
- The “corporate dominance” of Commission expert groups by industry representatives appearing in a “personal capacity”, using high-level access to influence EU policy.
- The increasing use of “Pharmish” – a form of “doublespeak” creeping from industry documents into EU rhetoric, which manipulates public understanding.
- How patients are effectively asked to fund drug “research” costs twice, as many costs are already covered by taxpayer-funded universities that often carry out research and development before pharma companies buy the rights.
Among
the EU laws targeted or shaped by the industry include rules around clinical
trials’ data transparency, trade secrets, and the negotiation of the EU-US
trade deal, the Transatlantic Trade and Investment Partnership (TTIP), the
report said.
A
total of 40 pharmaceutical companies now appear on the EU’s transparency
register – up from 23 in January 2012 with Bayer AG, GlaxoSmith-Kline and
Novartis topping the list, having spent €6.5m on lobbying last year alone.
Swiss pharmaceuticals giant Novartis' Basel
headquarters (Getty)
But under-reporting and the continued avoidance by some firms of the EU’s voluntary transparency system mean that overall big pharma lobbying outlay is likely to be much higher, CEO claims.
Efpia,
whose lobbying expenditure has gone from €50,000 in 2010 to more than €5m last
year, plays a “covert and explicit” role in shaping the policy agenda, by
sending lobbyists in a “personal capacity” to sit in on the Commission’s expert
groups, the report said.
But under-reporting and the continued avoidance by some firms of the EU’s voluntary transparency system mean that overall big pharma lobbying outlay is likely to be much higher, CEO claims.
Φαρμακευτικό Μάρκετινγκ: Θεωρία, Πρακτική, Δεοντολογία
Ζητήστε το στα κεντρικά βιβλιοπωλεία ή δώστε την παραγγελία σας τώρα…
The
ultimate guide for Pharma Marketing Champions
Ζητήστε το στα κεντρικά βιβλιοπωλεία ή δώστε την παραγγελία σας τώρα…
Efpia
representatives appear on official advisory bodies concerning alcohol and
health, corporate responsibility, and implications of patent law in
biotechnology and genetic engineering.
Efpia was yet to respond to the report last night. But with a record number of
drug patents set to expire over the next few years, allowing cheaper generic
drugs to be produced and threatening industry profits, the huge increase in
lobbying spending coincides with a critical time for the sector.
When
Pfizer’s patent for Viagra expired in 2013, the cost of a pill reduced in price
from £10 to around 85p. By 2019 other companies are predicted to lose more than
£40bn of combined income from their “blockbuster drugs”, according to research
firm GlobalData.
Industry
groups therefore want the bilateral EU-US TTIP trade agreement to ensure longer
monopoly periods and higher medicine prices for any exclusive medicines, the
report authors said.
The cost of Viagra reduced after Pfizer’s
patent expired (Getty)
They warned any provisions on intellectual property rights in the proposed free trade treaty would allow US pharmaceutical companies to sue EU member states over measures to promote access to medicines, such as price controls and stricter parliamentary standards, through a system of international-state dispute settlements.
They warned any provisions on intellectual property rights in the proposed free trade treaty would allow US pharmaceutical companies to sue EU member states over measures to promote access to medicines, such as price controls and stricter parliamentary standards, through a system of international-state dispute settlements.
“Such
provisions will intensify health inequalities, compromise access to affordable
medicines and hand more power and privilege to an increasingly unaccountable
industry,” the CEO report said.
The
settlements have already been used by big tobacco firms taking advantage of
similar bilateral trade agreements to sue countries who attempt to tighten
their smoking legislation.
Chancellor George Osborne looks through a
microscope at Pfizer's pharmaceutical science lab in 2011 (Getty)
Rachel Tansey, CEO researcher and author of the report, said: “The large-scale efforts of big pharmaceutical companies to mould EU policy to their own commercial benefit and their privileged access to EU decision-makers is deeply worrying.
Rachel Tansey, CEO researcher and author of the report, said: “The large-scale efforts of big pharmaceutical companies to mould EU policy to their own commercial benefit and their privileged access to EU decision-makers is deeply worrying.
“Strong
measures are needed to avoid capture of EU health policy by big pharma,
beginning with full transparency over industry lobbying and ending of
privileged access.”