Dunne: legal highs regime costs and penalties announced
Hon Peter Dunne
Associate Minister of Health
10 October 2012
Dunne: legal highs regime costs and penalties announced
Legal high manufacturers will face estimated $180,000 application fees plus $1 million to $2 million in testing costs for each product they want to sell, and up to eight years in prison for selling banned substances, Associate Health Minister Peter Dunne said today in announcing details of the permanent psychoactive substances regime.
“I make no apologies for setting the bar high on public safety and putting in place a regime with the process costs squarely on the legal highs industry, and not the taxpayer,” Mr Dunne said of the regime which should be in place by the middle of next year.
“I have said all along that this regime will be fundamentally based on reversing the onus of proof so those who profit from these products will have to prove they are as safe as is possible for psychoactive substances.
“We will no longer play the cat-and-mouse game of constantly chasing down substances after they are on the market.
Penalties under the new regime will include up to eight years in prison for importing, manufacturing, supplying or possession with intent to supply analogues of controlled drugs that come under the Misuse of Drugs Act, and up to two years for import, manufacture, supply or possession with intent to supply unapproved substances.
Other key features of the new regime that have been approved by Cabinet include:
• Personal possession of an unapproved product
will incur a $300 fine.
• There will be a minimum
purchase age of 18.
• No advertising except at point of
sale.
• Restrictions on outlets, including barring
dairies from selling such products, and labelling and
packaging requirements.
Mr Dunne said the $300 personal possession fine is deliberately not being legislated as a criminal offence.
“What we are trying to do is actually protect young people, not criminalise them and thereby jeopardise their job and travel prospects. The approach we are taking is similar to that used with alcohol infringements,” he said.
Labelling and packaging requirements will require all products to have a label listing their active ingredients, the phone number for the National Poisons Centre and contact details for the product’s New Zealand manufacturer or supplier.
‘To date, there has been no ingredient information, so no one who buys these products has the first clue what is in them, which is as ridiculous as it is dangerous and irresponsible,” Mr Dunne said.
“We have had considerable success with the Temporary Class Drug Notices that we instituted in August last year. They have taken 28 substances and more than 50 synthetic cannabis products off the market, but that was always a temporary measure until we could get this regime in place,” Mr Dunne said.
He said he will introduce the required legislation later this year and it is expected to be in place by the middle of next year. In the meantime, all existing temporary notices will be rolled over so they remain in effect until the permanent regime is in place.
The Cabinet paper and Regulatory Impact Statement can be found at www.health.govt.nz/about-ministry/legislation-and-regulation/regulatory-impact-statements/new-regulatory-regime-psychoactive-substances
Psychoactive Substances Regime Questions and Answers
What
are low risk psychoactive substances?
This refers to
new psychoactive substances for which the risks are low
enough that they meet the approval criteria set by the
regulatory. We say 'low-risk' to avoid implying that they
will be entirely safe, as there will always be some risk.
This is because different people have different reactions to
pharmacologically active substances.
Why is the
Government bringing in a psychoactive substances
regime?
We are doing this because the current
situation is untenable. Current legislation is ineffective
in dealing with the rapid growth in synthetic psychoactive
substances which can be tweaked to be one step ahead of
controls. Products are being sold without any controls over
their ingredients, without testing requirements, or controls
over where they can be sold. The government must prove a
risk of harm before controlling a substance. The new regime
will require a supplier or manufacturer to apply to a
regulator for a safety assessment before any product can be
sold.
Are we legalising drugs?
No. The regime
will provide stronger controls over psychoactive substances.
At the moment, these products are unregulated, with no
control over ingredients, place of sale, or who they can be
sold to. Because they are synthetic substances, there are a
huge number of potential ingredients, which makes it
unfeasible to deal with them individually.
It will be illegal to sell any product which has not been through an assessment. There will be strict restrictions on where products can be sold, the purchase age, and marketing restrictions.
What will the implications of the new
regime be for cannabis?
The legal status of cannabis
will not change. This is because the regime will only cover
new psychoactive substances that are not already classified
under the Misuse of Drugs Act 1975.
Why don’t you
just ban everything?
Legislation should not be used
to restrict behaviour that cannot be proved to be harmful.
Products that meet the approval criteria will be approved.
However, our position will still be that not using these
products is the safest option.
Is this a stealthy way
of banning everything and never approving any
product?
No. Clear testing requirements are being
established to determine the risks of psychoactive products.
Products that meet the approval criteria will be
approved.
How will risk/safety be
determined?
Consistent toxicological and behavioural
testing will be required for every product seeking approval.
A new regulator will be established to consider the data
from this testing for each product. Products that meet the
approval criteria will be approved.
What do you mean by
the regulator?
A regulator will need to be
established for psychoactive substances. This regulator will
oversee the approval of products, monitor for compliance
with post market restrictions, and reassess products in
light of any new evidence of harm that might arise.
How
many drugs will get approved?
We don’t know this
yet. Products that meet the approval criteria will be
approved. This will require toxicological and behavioural
testing.
Who will do the risk assessments?
The
new regulator will consider toxicological and clinical data
for each product.
Does this mean the Government is
endorsing drugs?
No. At the moment these products are
available without any information regarding their risks to
health. We are changing the system to require industry to
prove they do not pose a greater than a low risk of health
before they may be sold.
Will there be controls to stop
children buying these drugs from dairies?
Yes, it is
intended that there will be restrictions on where substances
can be sold and a minimum purchase age which will be set in
due course.
What happens when the legislation comes into force? Will everything be pulled from the shelves?
A transition period will follow enactment of
the new regime. During the transition period, a sponsor will
only be able to sell:
• products with an application
pending approval by the regulator; and
• that have been
legally on the market for at least six months prior to
enactment of the new regime; and
• provided that there
are no health concerns about the products
concerned.
Will this just backfire and create a bigger
black market?
No. We expect that having low risk
psychoactive products legally available will make it less
likely that consumers will resort to a black
market.
ENDS