health & consumer protection directorate general gmos: scientific disagreement or differing...
TRANSCRIPT
Health & Consumer ProtectionDirectorate General
GMOs: scientific disagreement or
differing societal perceptions?
Marco Valletta, Ph. D. – DG SANCO E1
OECD 2-3 November 2009
Consumers’ perception and GMOs in the EU
A recent study from the University of Wageningen – by Professor Lynn J. Frewer
Consumers not willing to seek information
Adequate Risk management and happy consumers
More acceptance of economic interests
Emphasise state and industry
Negative view - create public anxiety
Inherent in science
Poor quality of information
Opaque / lack of trust
Less acceptance of economic interests
Emphasise consumer protection
Positive view – reliable
Not acknowledged by all institutions – source of
negative perceptions
Krystallis et al, 2007, Health, Risk & Society
Consumers Experts
Risk management
efforts
Risk management
priorities
Responsibility
Media
Uncertainty
Consumer Awareness
Some basics about risk perception by consumers
Losses have greater impact on attitudes than gains (Kahneman and Tversky, 1979).
People weigh risk information as more important than benefit information
Impact of balanced information higher on risk perception than on benefit perception (Fischer and Frewer)
Risk perception in food technologies
Consumer attitudes to new food technologies “not starting from zero” – food has always been there not like pharma
Consumers make trade-offs between risk, benefit and cost (including ethical & environmental costs)
Consumer decisions are made on a case-by-case basis related to specific perceptions of risk and benefit
Consumers’ decisions and perceptions might be (very) far from a rationale science-based approach
What went wrong with GM food Resistance based on perceived risk GM food perceived as unnatural and therefore risky Uncontrollable by those exposed to them Food is a special cause of concern (taken into the body) Unknown long-term risks Substantial equivalence did not address consumer concerns Opaque risk analysis systems and decision-making practices
were not helpful
Resistance based on values and benefit analysis Consumer choice issue: has to do with marketing more than
with ideology (“who wants what and why?”) Food a special issue in Europe No consumer benefits from the 1st generation of GMOs Who is getting the final benefits (Third Countries farmers?
Biotech companies?) Impact on biodiversity Ethical doubts
The objectives of the European Legislation
Managing possible risks
Foster innovation
Protect consumers’ right to know and
choose
Avoid trade barriers
After the food scandals of the 90s a new regulatory framework
Directive 2001/18 on the deliberate release of GMOs into the environment
Regulation (EC) No 1829/2003
on GM food and feed
Regulation (EC) No 1830/2003
on traceability and labelling of GMOs
The EU model approach
RA and RM as separate steps
Risk assessment: European Food Safety Authority
Risk management: European Commission through a regulatory committee procedure
A fully transparent process open to 27 MS of the EU and to more than half a billion EU citizens
EFSA risk assessmentFully independent from the political levelRA based on international standardsSome of the best scientists in the EU selected ad hoc (GM Panel + expert + EFSA staff)The three typical steps of RA
Compositional analysisFood and feed safety analysisEnv. impact analysis
+ a wide consultation with 27 MS scientific bodiesDefined as the most comprehensive (and longest) RA process in the world
Risk management phase
Comm. / EFSAMS Working group
Commission Proposal of Decision
Comments from The publicStanding Committee (SCFCAH – GMFF)
Opinion, 3 months after EFSA’s opinion
Commission
In favour, QM
EFSA’s Final opinion
Commission decision - Publication in OJ- Inclusion in GMO register
No Opinion
Council, 3 monthsNo opinion /In favour, QM
Against, QM
Commission to redraft the proposal
Against, QM
Elements to reassure consumersAuthorisation
Granted for 10 yearsCan be reviewed/withdrawn at any momentRenewable for 10-year periodsAlways for food and feed (no Starlink case in the EU)
Authorization holder responsible for safety, post market monitoring
Authorised products are entered in the Community register containing all relevant info
http://ec.europa.eu/food/dyna/gm_register/index_en.cfm
Consumer information - labelling Compulsory for food/feed contain, consist of, produced
from GMOs regardless of the presence of modified DNA or proteins
In the list of ingredients if pre-packaged Otherwise visible if non pre-packed
0,9% threshold for adventitious presence of authorised GMOs (operators responsible to take measures)
Lower levels may be adopted via comitology
- National provision for GM-free labels and for menus- NOT for products obtained from animals fed with GM feed or
treated with GM medicines (eggs, milk, meat) but the issue is becoming more and more important and often addressed at private level
Consequences of the EU legislation
More than 25 GMOs authorised in the EU
10 new GM food and feed authorised under the new regulatory framework (not for cultivation)
55 requests pending (15 cultivation)
EU: second in the world for number of GM authorisations granted
….and yet EU consumers perception is rather negative although gradually improving
Winning consumers’ trust by improving what the way we do what we do
Shared guidelines for RA (Comm, EFSA, MS in consultation with stakeholders)
An evaluation of the existing legislation
The risk assessment and regulatory approval process
The labelling rules on GM food and feed
Consumers’ acceptance
Discussion on integrating other legitimate factors in the author. process
ConclusionsConsumers have views which are the result of different factors and might diverge from scientific objectivity
Scientists should keep delivering the best possible independent risk assessment
Policy makers: not just implementer of science but a bridge between consumers and scientists
The EU model tries to apply this approach
Results have been encouraging but more time and more action is needed
Finding the right balance on this and other controversial issues might imply re-thinking our approach to policy making