René Crevel -...
Transcript of René Crevel -...
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PRECAUTIONARY ALLERGEN LABELLING – HOW CAN PAL REFLECT ACTUAL RISK?
Food Matters Live ExCeL London 22-24 November 2016
René Crevel
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OUTLINE
• Precautionary allergen labelling: current
perspectives
• Risk and risk assessment
• Are we there yet?
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…… PRECAUTIONARY (ADVISORY – “MAY
CONTAIN”) ALLERGEN LABELLING
• Introduced in the 1990s
• First suggested by CFIA/Health
Canada
• Voluntary
• Twin roles, closely intertwined
• Risk management and risk communication
• Effective outcome: people at risk avoid the
product
• Ineffective outcome: people at risk don’t believe
it and/or are confused by it and disregard it
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THE PROBLEM WITH
PRECAUTIONARY LABELLING TODAY
»Numerous phrases with different risk
implications (although not necessarily
associated with real differences in levels of risk)
»Lack of transparency over its application
• No generally agreed set of reference values as
the basis for precautionary labelling
• Risk assessment process often unclear
»Allergic consumers are confused and many do
not trust precautionary labelling
»Significant numbers ignore it at least part of the
time, putting themselves at risk
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VARIETY OF PAL PHRASES
Survey of allergen advisory labelling and allergen content of UK retail pre-
packed processed foods – Report for FSA by RSSL (2014)
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PAL PHRASES: FURTHER VARIATIONS
ON A THEME OF “MAY CONTAIN”
and many more
Survey of allergen advisory labelling and allergen content of UK retail pre-packed
processed foods – Report for FSA by RSSL (2014)
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…… PRECAUTIONARY (ADVISORY – “MAY CONTAIN”)
ALLERGEN LABELLING TODAY - SUMMARY
• No consistent standards for
application:
use dependent on internal
company standards and
perception of risks
• Negative perception by
consumers and health care
practitioners
• Result: misunderstanding and
mistrust, lack of observance and
consequently higher risks to
allergic consumers
1 Annex II food 10 Annex II foods
PAL statement not
expected on
product
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PAL IS NOT MEETING ITS OBJECTIVES
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0%10%20%30%40%50%60%70%80%90% Ben-Shoshan et al. JACI (2012) 129: 1401
Never purchase if labelled
0%
5%
10%
15%
20%
25%
30%
35%
40% Cochrane et al. Clin Trans Allergy (2013) 3: 31.
• Allergic consumers are disregarding PAL
statements to a significant extent
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WHAT DOES/CAN A PAL STATEMENT MEAN?
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Dunngalvin A, Chan CH, Crevel R et al. Precautionary Allergen Labelling:
Perspectives from key stakeholder groups. Allergy 2015, 70, 1039-1051
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RISK AND RISK
ASSESSMENT
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• The answer is in the question (at least partly):
Base it on risk
• Some considerations
• What is risk?
• What risk are we talking about?
• What do we need to know in order to base PAL
on risk?
SO HOW CAN PAL REFLECT ACTUAL RISK?
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WHAT DO WE MEAN BY RISK?
Fundamental principle of toxicology:
“The dose makes the poison” (Paracelsus, 15th Century)
Implication: the key parameter is risk not hazard
Risk »the likelihood that, under particular conditions of exposure, an
intrinsic hazard will represent a threat to human health.
» Risk = f (hazard, exposure)
with a consideration of the nature of the effects
Characterising the hazard is therefore a critical step
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FOOD ALLERGENS: DOSE AND EFFECT
Considerations
- Zero risk does not exist in practice
- What is an acceptable/tolerable risk?
- In terms of the nature (severity) of the effects?
- In terms of the frequency of effects (how many will be affected)?
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RISK ANALYSIS IN FOOD
Three parts
Interactive and iterative process
Risk Analysis
Risk Assessment
Risk Management
Risk Communication
©2016
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ASSESSING THE RISK FROM FOOD
ALLERGENS: HOW MUCH IS TOO MUCH?
What is the relationship
between dose and frequency /
severity of response?
How many people are likely to
suffer a reaction, and how severe
will the reaction be?
How much are people
exposed to?
Risk
characterisation Hazard
identification
Exposure
assessment
Hazard
characterisation What is the toxicological
concern?
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PEANUT DOSE DISTRIBUTION:
CHARACTERIZING THE HAZARD
17
Cum
ula
tive P
erc
enta
ge o
f R
esponses
0%
10%
20%
30%
40%
50%
60%
70%
80%
90%
100%
Log-Normal Dose of Protein (mg)
0.01 0.1 1 10 100 1000 10000 100000
Discrete Cumulative
ED 01
ED 05
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VITAL SCIENTIFIC EXPERT PANEL RECOMMENDATIONS
AND PROPOSED ACTION LEVELS.
Allergen Basis of
reference dose
Reference dose
(mg Protein)
50 g Serving
Size: Action
Level (ppm)
250 g Serving
Size: Action
Level (ppm)
Peanut ED01 0.20 4.0 0.80
Milk ED01 0.10 2.0 0.40
Egg ED01 0.03 0.6 0.12
Hazelnut ED01 0.10 2.0 0.40
Soy ED05 95LCI 1.00 20.0 4.00
Wheat ED05 95LCI 1.00 20.0 4.00
Cashew ED05 95LCI 2.00 40.0 8.00
Mustard ED05 95LCI 0.05 1.0 0.20
Lupin ED05 95LCI 4.00 80.0 16.00
Sesame ED05 95LCI 0.20 4.0 0.80
Shrimp ED05 95LCI 10.00 200.0 40.00
Celery Insufficient data
Fish Insufficient data
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1
9
VITAL 2.0 REFERENCE DOSES
»Defined by reference to population health-
based outcomes (proportion likely to react)
»Serve as benchmarks for allergen management
• Define what is judged safe
• Define when additional risk management
measures are required e.g. PAL
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RISK ASSESSMENT: EXPOSURE
Crevel RWR, Baumert JL, Baka A, Houben GF, Knulst AC, Kruizinga AG, Luccioli
S, Taylor SL, Madsen CB. Development and evolution of risk assessment for food
allergens. Food Chem Tox (2014) 67, 262-276.
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HOW SAFE ARE VITAL 2.0 REFERENCE
DOSES: SINGLE DOSE CHALLENGES
2
1
• Concept
• Run in routine allergy clinics
• Challenge every patient attending for
the food allergy of interest (no exclusions)
• Single dose – ED05 selected as balance
between good safety and numbers
needed to be challenged for statistical
robustness
• Open challenges
• Information generated for risk assessment
• Validation of ED05 derived from dose distribution
modelling
• Severity profile at ED05
ED05
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SINGLE DOSE CHALLENGES:
PEANUT STUDY
2
2
• 375 clinic attendees with peanut allergy
• Three centres: Cork, Melbourne, Boston
• 6mg whole peanut in a cookie (except for
participants allergic to other ingredients in the
cookie)
• Open challenge
• 2-hour post-challenge follow-up
• Data support the VITAL ED05 value of 1.5mg for
peanut protein
Full results expected to be published soon!
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ARE WE THERE YET?
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Chapter V. Article 36
“3. The Commission shall adopt implementing acts on the application of the
requirements referred to in paragraph 2 of this Article to the following voluntary food
information:
(a) information on the possible and unintentional presence in food of substances
or products causing allergies or intolerances;”
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NEW REQUIREMENTS FOR VOLUNTARY
ALLERGEN INFORMATION (REG 1169/2011)
Precautionary labelling remains voluntary (Article 36)
»However mandatory requirements are introduced (e.g. name of
allergenic food)
»Specific rules apply:
“2. Food information provided on a voluntary basis shall meet
the following requirements:
(a) it shall not mislead the consumer, as referred to in Article 7;
(b) it shall not be ambiguous or confusing for the consumer;
and
(c) it shall, where appropriate, be based on the relevant
scientific data.”
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WHAT COULD IT ALL MEAN?
(a) shall not mislead: PAL should be accurate, i.e.
use must be justified
(b)shall not be ambiguous or confusing:
terminology should be clear and limited to one
(or a few) well-understood terms
(c) be based on the relevant scientific data: PAL
should be based on a thorough risk assessment
(preferably quantitative)
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DG SANTE-JRC STAKEHOLDER WORKSHOP
(GEEL, BELGIUM 16-17 JUNE 2016)
Participants (46): Delegates (19) from Member States' competent
authorities and delegates representing relevant stakeholders (e.g.
FoodDrinkEurope and the European Federation of Allergy and Airways
Disease Patients Association).
AIMS (provided by DG SANTE-JRC)
»Background: Regulation (EU) 1169 /2011 on the provision of
food information to consumers and the observed proliferation
of precautionary allergen labelling by food producers.
»To identify the sequence of steps required for framing the
current use of precautionary allergen information and its
enforcement across the EU.
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DG SANTE-JRC STAKEHOLDER WORKSHOP
(GEEL, BELGIUM 16-17 JUNE 2016)
Agenda
SESSION 1: Legislative and Allergy Sufferers Requirements (DG SANTÉ,
EFA)
SESSION 2: Risk Based Approaches to Allergen Management
(FoodDrinkEurope, iFAAM)
SESSION 3: The Role of Analysis in Enforcing Legislation (JRC-IRMM)
» Breakout groups after each session
SESSION 4: Conclusions from Discussion Topics
» Topic 1: Legislative perspective on precautionary labelling, its current wording and conditions of
use
» Topic 2: Risk based approaches
» Topic 3: Comparing results from analytical measurements
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DG SANTE-JRC STAKEHOLDER WORKSHOP
(GEEL, BELGIUM 16-17 JUNE 2016):
CONCLUSIONS 1
Legislative perspective on precautionary labelling, its current wording and
conditions of use.
» PAL terminology: should be simple, easy for consumers to understand
• “may contain” recommended
» Use of PAL should be subject to defined conditions and transparent:
» Documented risk assessment
» Allergen management procedures in place
» No PAL statement below reference dose
» Benchmarks need to balance degree of protection/safety and choice for
allergic consumerss (reference doses) need endorsement by EFSA
» Communication to users (both consumers and health care practitioners) is
crucial
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DG SANTE-JRC STAKEHOLDER WORKSHOP
(GEEL, BELGIUM 16-17 JUNE 2016):
CONCLUSIONS 2
Risk-based approaches »Guidance on good risk assessment practice EU-wide required
»Protein is the hazard and should be basis of the risk assessment
»Stakeholders want acceptance (by the authorities) of the RDs defined
by VITAL
» They wish to encourage FBOs to use them and evaluate how well they work.
»Commission role to develop a framework based on general principles
» detail to be developed by other stakeholders (e.g. authorities, trade associations)
»Questions on readiness of FBOs for application of RDs (VITAL/iFAAM)
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DG SANTE-JRC STAKEHOLDER WORKSHOP
(GEEL, BELGIUM 16-17 JUNE 2016):
CONCLUSIONS 3
Comparing results from analytical measurements
» Expressed results in units that can be directly applied to the risk assessment,
i.e. mg total protein/kg of food
» This links analysis to the materials used for clinical food challenges.
» Could be looked at in the context of Infrastructure to support framework:
• existing structures may provide a possible model e.g. Veterinary Medicines
» Priority allergens: wheat, milk and egg, based on frequency of RASFF
notifications for these allergens
» Guidance to good analytical practice for food allergens should be developed
• Nordic group could lead, based on their experience
» Further workshops likely needed as work developed
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CONCLUDING REMARKS
Precautionary allergen labelling (PAL) continues to fail
allergic consumers
PAL needs to be based on transparent, understood and
accepted risk assessment
The VITAL 2.0 scheme proposed scientifically sound and
transparent reference doses, based on a human data which
form a basis for this risk assessment
Developing scientific and regulatory perspectives offer
opportunities to introduce a robust framework for the
application of PAL
Acting on these opportunities can restore the value of PAL
and thereby help allergic consumers as well as FBOs
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THANK YOU FOR YOUR ATTENTION
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Seven secrets to successful nutritional
labelling …….
…..and the seven sins commonly made with
health and nutrition claims
Mike Peters Dr Andy Bowles
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Seven secrets to
successful nutritional
labelling – Mike Peters
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Despite
Brexit !
Nutritional labelling is here to stay!
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What’s in a label – take
a holistic approach!
Product Development
Portion &
cooking instructions
Fortification
Functional
Formulation
Nutrient reduction
or increase
On pack comments/claims
Food trends
Widen appeal
Nutritional analysis
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The UK’s nutrition imbalance
*Vitamin A, riboflavin, iron, calcium,
magnesium, potassium, zinc, iodine
Not
enough F&V, Fibre
Omega 3
Vitamins/
minerals*
Too much Saturated fat
Sugar
Salt
Weight!
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Sampling Matters!
Egg Milk Rye Wheat Biscuits French
beans
No. of labs 18 18 19 19 19 18
Mean
(g/100g dry wt)
37.8 27.3 2.6 3.0 11.6 2.7
Range 29.4-44.2 24.5-30.0 1.6-4.5 1.8-5.8 9.9-15.4 1.2-5.8
CV (within) 2.0 2.0 24.5 30.6 2.7 25.7
CV (between) 8.7 5.4 36.4 29.3 10.3 54.0
• Within labs the same methods are
used
• Different labs use different methods
• Less repeatable at lower
concentrations
• Less accurate at lower
concentrations
Eurofoods trial 1985: Leading European laboratories
Hollman & Katan, 1988, Journal of the American Medical Association
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Variation in nutrient content of foods
Natural variation Extrinsic differences
• Different animals/plants
• Season
• Feeding regime
• Country of origin
• Growing conditions
• Storage
• Change in recipe
• Fortification practices
• Home prepared dishes not
regulated
• Length of cooking time
• Water used to cook with
• Cooking utensils
Analytical values are a snapshot of what was analysed and composition of
any individual sample may differ considerably. There are two main reasons
for the variability, in addition to analytical variation.
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Vitamin and mineral declarations
The following vitamins and minerals may be added to the
nutrition table but only if they are present in significant
amounts
Vitamin A (µg) Folic acid (µg) Iron (mg)
Vitamin D (µg) Vitamin B12 (µg) Zinc (mg)
Vitamin E (mg) Biotin (µg) Copper (mg)
Vitamin K (µg) Pantothenic acid (mg) Manganese (mg)
Vitamin C (mg) Potassium (mg) Fluoride (mg)
Thiamin (mg) Chloride (mg) Selenium (µg)
Riboflavin (mg) Calcium (mg) Chromium (µg)
Niacin (mg) Phosphorus (mg) Molybdenum (µg)
Vitamin B6 (mg) Magnesium (mg) Iodine (µg)
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See the bigger picture coming!
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Seven sins commonly made with
health and nutrition claims
Dr Andy Bowles Specialist food law solicitor
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Health and Nutrition claims
Nutrition claims
Energy
Nutrition
Health claims Any statement about a relationship between food and health
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Health claims – the law
Types of health claims
“Function”
“Risk reduction”
“Childrens development”
Non-specific health claims
Only made where approved health claim listed
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Register of nutrition and health claims http://ec.europa.eu/nuhclaims/
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Other claims
“Natural”
“Fresh”
“Traditional”
“Home made”
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Main principles
Claims must be
Substantiated
Accurate
Truthful
Not misleading
Not just on labels!
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Most common sins…
1. “Packed with..” “bursting with….” for source of
claims.
2. Non-specific health claims “Good for you”
3. Health claims on unhealthy foods.
4. “Natural” with refined ingredients
5. “Free from” – applies to all similar products
6. Non- approved health claims.
7. Non-approved wording.
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Come and see us…
ABC Food Law – Stand 592
ABC Legal Labels – Stand 642
IFR Extra - Stand RP20
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Our Contact Details
Name &
Company
Contact Details What we can help you with
Mike Peters
Nutritional
Information
Solutions
Tel 01603 251431/07894 851527
www.nutritionalinformation.solutions
• Inexpensive nutrition label
information from your product
recipe, for front and back of pack,
independently checked and
verified to meet regulations
Dr Andy Bowles
ABC Food Law
Tel: 01603 274486
www.abcfoodlaw.co.uk
www.abc-legal-labels.co.uk
@abcfoodlaw
• Any food law issue including
• Food label/reviews
• HACCP
• Allergen control
• Import/export
• Traceability
• Novel foods
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The impact of EU FIC Regulation for business and consumers
Sarah Howarth 22nd November 2016
www.howarthfoodsafety.co.uk
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Agenda
www.howarthfoodsafety.co.uk
• Impact • Implementation • Enforcement • Conclusions
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Aims of EU No 1169/2011
- A harmonised approach across the EU
- Free movement of safe and wholesome
food
- Allow more informed consumer choice
- Drive healthier food choices
- Simplify legislation
•
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Impact for business
www.howarthfoodsafety.co.uk
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Significant changes
Name of the Food List of Ingredients Naming of certain ingredients/categories Quantity of certain ingredients Allergens Nutritional information Net quantity of the food Date of minimum durability Special storage conditions/conditions of use Business name (FBO) and address in the EU Font size Distance selling Country of Origin
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Impact for business
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EU No 1169/2011Timescales
30 January 2008:
Commission proposal
24 Oct 2011:
Published
13 Dec 2014:
Application
Further reports
2013 : meat ingredients
2015 : TFA’s ; extension
COOL
13 Dec 2016:
Mandatory Nutritional information
www.howarthfoodsafety.co.uk
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Key ingredients for implementation
New Label
Marketing and Sales
FIC Guidance
Supplier/manufacturing information
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Common challenges
• Lack of clarity and guidance on the changes • Resources - budget ; skills ; time • Delay in obtaining supplier information • Inadequate in-house data/specifications • Amending internet sites • Fitting all mandatory information on pack • Packaging right-offs
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Common areas of confusion
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Allergens ????
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Enforcement officers
www.howarthfoodsafety.co.uk
- Possess guidance to determine and ensure that their actions are reasonable, proportionate and commensurate with good practice
- Use a gradual and educative approach UNLESS they determine that there is Significant Risk for the public
- May move to formal actions if the desired change is not achieved in a reasonable time period
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Where are we now? - Business
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Understanding NI Consumer Needs Around Food Labelling (July 2016)
Overall, participant attention to labelling information appeared to be driven by a particular need; for example, if participants were following a specific diet or had specific dietary or allergen requirements. Outside of these circumstances, participants tended only to use labels to check the “use by” or “best before” dates, and occasionally checked labels when buying new or unfamiliar products.
Source : FSA Website
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Conclusions - Have the aims of EU No 1169/2011 been achieved?
- A harmonised approach across the EU
- Free movement of safe and wholesome
food
- Allow more informed consumer
choice
- Drive healthier food choices
- Simplify legislation
•
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Impact for Consumers?
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Thank you!