Foram encontradas 1.218 questões.
O Brasil encontra-se em um processo de eliminação do sarampo e o sistema de vigilância desempenha um papel importante para alcançar essa meta. Sobre esse assunto, julgue os itens que se seguem.
A subnotificação é uma característica intrínseca do sistema de vigilância ativa que tem impacto negativo sobre a oportunidade das estratégias de controle.
Provas
In 2004, the General Food Regulation (GFR) is
being made under the food safety Act 1990, in order to
allow greater flexibility in relation to penalties for offences.
Their main purpose is to provide new enforcement
powers in respect of new obligations relating to food and
food businesses, to apply from January 1 , 2005 underst
Regulation 178/2002. These are:
Article 14 – Food Safety Requirement. This prohibits food
being placed on the market if it is unsafe, and specifies
what this means.
Article 16 – Presentation. This stipulates that the labeling,
advertising and presentation of food shall not mislead
consumers.
Article 18 – Traceability. This requires food businesses to
keep records of their suppliers and businesses they supply
to, and to make such records available to competent
authorities on demand.
Article 19 – Product Recall/W ithdrawal. This places
obligations on food business to recall, and/or withdraw
food from the market if it is not in compliance with food
safety requirements, and to notify competent authorities.
The regulations designate food authorities, port
health authorities and the Food Standards Agency (FSA)
as the relevant competent authorities and enforcement
bodies. The FSA has been included as an additional
enforcement body in respect of Articles 14 and 19 in
certain circumstances. This is to allow, for example, for the
flexibility of the Meat Hygiene Service enforcing these
requirements in meat plants, where this should be more
effective.
Internet: www.food.gov.uk/foodindustry (with adaptations)
Based on the text above, judge the following items.
The expression “meat plants” (l.29) means carnivorous plants.
Provas
In 2004, the General Food Regulation (GFR) is
being made under the food safety Act 1990, in order to
allow greater flexibility in relation to penalties for offences.
Their main purpose is to provide new enforcement
powers in respect of new obligations relating to food and
food businesses, to apply from January 1 , 2005 underst
Regulation 178/2002. These are:
Article 14 – Food Safety Requirement. This prohibits food
being placed on the market if it is unsafe, and specifies
what this means.
Article 16 – Presentation. This stipulates that the labeling,
advertising and presentation of food shall not mislead
consumers.
Article 18 – Traceability. This requires food businesses to
keep records of their suppliers and businesses they supply
to, and to make such records available to competent
authorities on demand.
Article 19 – Product Recall/W ithdrawal. This places
obligations on food business to recall, and/or withdraw
food from the market if it is not in compliance with food
safety requirements, and to notify competent authorities.
The regulations designate food authorities, port
health authorities and the Food Standards Agency (FSA)
as the relevant competent authorities and enforcement
bodies. The FSA has been included as an additional
enforcement body in respect of Articles 14 and 19 in
certain circumstances. This is to allow, for example, for the
flexibility of the Meat Hygiene Service enforcing these
requirements in meat plants, where this should be more
effective.
Internet: www.food.gov.uk/foodindustry (with adaptations)
Based on the text above, judge the following items.
The FSA has the power to control and check the way the food industry operates and to provide it with technical expertise, imposing fines or penalties on those businesses that break the law is also part of its job.
Provas
In 2004, the General Food Regulation (GFR) is
being made under the food safety Act 1990, in order to
allow greater flexibility in relation to penalties for offences.
Their main purpose is to provide new enforcement
powers in respect of new obligations relating to food and
food businesses, to apply from January 1 , 2005 underst
Regulation 178/2002. These are:
Article 14 – Food Safety Requirement. This prohibits food
being placed on the market if it is unsafe, and specifies
what this means.
Article 16 – Presentation. This stipulates that the labeling,
advertising and presentation of food shall not mislead
consumers.
Article 18 – Traceability. This requires food businesses to
keep records of their suppliers and businesses they supply
to, and to make such records available to competent
authorities on demand.
Article 19 – Product Recall/W ithdrawal. This places
obligations on food business to recall, and/or withdraw
food from the market if it is not in compliance with food
safety requirements, and to notify competent authorities.
The regulations designate food authorities, port
health authorities and the Food Standards Agency (FSA)
as the relevant competent authorities and enforcement
bodies. The FSA has been included as an additional
enforcement body in respect of Articles 14 and 19 in
certain circumstances. This is to allow, for example, for the
flexibility of the Meat Hygiene Service enforcing these
requirements in meat plants, where this should be more
effective.
Internet: www.food.gov.uk/foodindustry (with adaptations)
Based on the text above, judge the following items.
Article 19 refers to the obligation of food businesses to improve and rearrange all the products that were not manufactured according to the rules of the Food Safety Act before displaying them again on the shelves of their shops.
Provas
In 2004, the General Food Regulation (GFR) is
being made under the food safety Act 1990, in order to
allow greater flexibility in relation to penalties for offences.
Their main purpose is to provide new enforcement
powers in respect of new obligations relating to food and
food businesses, to apply from January 1 , 2005 underst
Regulation 178/2002. These are:
Article 14 – Food Safety Requirement. This prohibits food
being placed on the market if it is unsafe, and specifies
what this means.
Article 16 – Presentation. This stipulates that the labeling,
advertising and presentation of food shall not mislead
consumers.
Article 18 – Traceability. This requires food businesses to
keep records of their suppliers and businesses they supply
to, and to make such records available to competent
authorities on demand.
Article 19 – Product Recall/W ithdrawal. This places
obligations on food business to recall, and/or withdraw
food from the market if it is not in compliance with food
safety requirements, and to notify competent authorities.
The regulations designate food authorities, port
health authorities and the Food Standards Agency (FSA)
as the relevant competent authorities and enforcement
bodies. The FSA has been included as an additional
enforcement body in respect of Articles 14 and 19 in
certain circumstances. This is to allow, for example, for the
flexibility of the Meat Hygiene Service enforcing these
requirements in meat plants, where this should be more
effective.
Internet: www.food.gov.uk/foodindustry (with adaptations)
Based on the text above, judge the following items.
“Traceability” (l.14) refers to the ability to find the records of food businesses or suppliers, in case competent authorities need to check them.
Provas
In 2004, the General Food Regulation (GFR) is
being made under the food safety Act 1990, in order to
allow greater flexibility in relation to penalties for offences.
Their main purpose is to provide new enforcement
powers in respect of new obligations relating to food and
food businesses, to apply from January 1 , 2005 underst
Regulation 178/2002. These are:
Article 14 – Food Safety Requirement. This prohibits food
being placed on the market if it is unsafe, and specifies
what this means.
Article 16 – Presentation. This stipulates that the labeling,
advertising and presentation of food shall not mislead
consumers.
Article 18 – Traceability. This requires food businesses to
keep records of their suppliers and businesses they supply
to, and to make such records available to competent
authorities on demand.
Article 19 – Product Recall/W ithdrawal. This places
obligations on food business to recall, and/or withdraw
food from the market if it is not in compliance with food
safety requirements, and to notify competent authorities.
The regulations designate food authorities, port
health authorities and the Food Standards Agency (FSA)
as the relevant competent authorities and enforcement
bodies. The FSA has been included as an additional
enforcement body in respect of Articles 14 and 19 in
certain circumstances. This is to allow, for example, for the
flexibility of the Meat Hygiene Service enforcing these
requirements in meat plants, where this should be more
effective.
Internet: www.food.gov.uk/foodindustry (with adaptations)
Based on the text above, judge the following items.
Article 16 of the GFR states that consumers should categorically refuse food products that make false promises or display dishonest claims.
Provas
In 2004, the General Food Regulation (GFR) is
being made under the food safety Act 1990, in order to
allow greater flexibility in relation to penalties for offences.
Their main purpose is to provide new enforcement
powers in respect of new obligations relating to food and
food businesses, to apply from January 1 , 2005 underst
Regulation 178/2002. These are:
Article 14 – Food Safety Requirement. This prohibits food
being placed on the market if it is unsafe, and specifies
what this means.
Article 16 – Presentation. This stipulates that the labeling,
advertising and presentation of food shall not mislead
consumers.
Article 18 – Traceability. This requires food businesses to
keep records of their suppliers and businesses they supply
to, and to make such records available to competent
authorities on demand.
Article 19 – Product Recall/W ithdrawal. This places
obligations on food business to recall, and/or withdraw
food from the market if it is not in compliance with food
safety requirements, and to notify competent authorities.
The regulations designate food authorities, port
health authorities and the Food Standards Agency (FSA)
as the relevant competent authorities and enforcement
bodies. The FSA has been included as an additional
enforcement body in respect of Articles 14 and 19 in
certain circumstances. This is to allow, for example, for the
flexibility of the Meat Hygiene Service enforcing these
requirements in meat plants, where this should be more
effective.
Internet: www.food.gov.uk/foodindustry (with adaptations)
Based on the text above, judge the following items.
Article 14 of the GFR explains why a given kind of food is not good for human consumption.
Provas
Hypoallergenic cosmetics
For the past four years, the Food and Drug
Administration (FDA) has been working to clear up this
confusion of claims by establishing testing requirements that
would determine which products really are hypoallergenic. But
late last year, the U.S. Court of Appeals for the District of
Columbia ruled that FDA’s regulation defining hypoallergenic
was invalid. This means there is now no regulation specifically
defining or governing the use of the term hypoallergenic or
similar claims. And because of the lengthy procedural steps
required to establish a new regulation that is likely to be the
situation for some time to come.
Where does that leave consumers?
Consumers concerned about allergic reactions from
cosmetics should understand one basic fact: there is no such
thing as a non-allergenic cosmetic — that is, cosmetic that can
be guaranteed never to produce an allergic reaction.
By and large, the basic ingredients in so-called
hypoallergenic cosmetics are the same as those used in other
cosmetics sold for the same purposes. Years ago, some
cosmetics contained harsh ingredients that had a high potential
for causing adverse reactions. B ut these ingredients are no
longer used. FDA knows of no scientific studies which show
that hypoallergenic cosmetics or products making similar
claims actually cause fewer adverse reactions than competing
conventional products.
Margaret Morrison. Internet: www.fda.gov (with adaptations).
Based on the text above, judge the following items.
The word “actually” (l.24) means indeed, in point of fact, in reality, really.
Provas
Hypoallergenic cosmetics
For the past four years, the Food and Drug
Administration (FDA) has been working to clear up this
confusion of claims by establishing testing requirements that
would determine which products really are hypoallergenic. But
late last year, the U.S. Court of Appeals for the District of
Columbia ruled that FDA’s regulation defining hypoallergenic
was invalid. This means there is now no regulation specifically
defining or governing the use of the term hypoallergenic or
similar claims. And because of the lengthy procedural steps
required to establish a new regulation that is likely to be the
situation for some time to come.
Where does that leave consumers?
Consumers concerned about allergic reactions from
cosmetics should understand one basic fact: there is no such
thing as a non-allergenic cosmetic — that is, cosmetic that can
be guaranteed never to produce an allergic reaction.
By and large, the basic ingredients in so-called
hypoallergenic cosmetics are the same as those used in other
cosmetics sold for the same purposes. Years ago, some
cosmetics contained harsh ingredients that had a high potential
for causing adverse reactions. B ut these ingredients are no
longer used. FDA knows of no scientific studies which show
that hypoallergenic cosmetics or products making similar
claims actually cause fewer adverse reactions than competing
conventional products.
Margaret Morrison. Internet: www.fda.gov (with adaptations).
Based on the text above, judge the following items.
Scientists’ lack of interest in the cosmetics industry in general leads to their failure to produce or publish studies that would conclusively solve the polemic surrounding “hypoallergenic” products.
Provas
Hypoallergenic cosmetics
For the past four years, the Food and Drug
Administration (FDA) has been working to clear up this
confusion of claims by establishing testing requirements that
would determine which products really are hypoallergenic. But
late last year, the U.S. Court of Appeals for the District of
Columbia ruled that FDA’s regulation defining hypoallergenic
was invalid. This means there is now no regulation specifically
defining or governing the use of the term hypoallergenic or
similar claims. And because of the lengthy procedural steps
required to establish a new regulation that is likely to be the
situation for some time to come.
Where does that leave consumers?
Consumers concerned about allergic reactions from
cosmetics should understand one basic fact: there is no such
thing as a non-allergenic cosmetic — that is, cosmetic that can
be guaranteed never to produce an allergic reaction.
By and large, the basic ingredients in so-called
hypoallergenic cosmetics are the same as those used in other
cosmetics sold for the same purposes. Years ago, some
cosmetics contained harsh ingredients that had a high potential
for causing adverse reactions. B ut these ingredients are no
longer used. FDA knows of no scientific studies which show
that hypoallergenic cosmetics or products making similar
claims actually cause fewer adverse reactions than competing
conventional products.
Margaret Morrison. Internet: www.fda.gov (with adaptations).
Based on the text above, judge the following items.
Nowadays manufacturers of cosmetics select the ingredients of their products more carefully than they did in the past.
Provas
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