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MILLAR
KREKLEWETZ
LLP is a boutique Canadian law firm with lawyers who have
significant expertise in assisting businesses dealing with
products regulated under Canada’s Food and Drugs Act (including vitamins, supplements, and other
natural health products), particularly in the direct selling
context (an area where we also possess significant expertise).
The
following is a short introduction to Food
and Drugs Act matters and to our services in this area.
Food and Drugs Act Matters
A wide range of health products commonly
available in the market-place today are regulated under
Canada
’s Food and Drugs Act
as “natural health products” (or “NHPs”).
Typical NHPs include vitamins, minerals, essential fatty
acids, health products made from plant materials and their
extracts, homeopathic and traditional medicines.
In order to import and sell NHPs in Canada,
companies must comply with the requirements of Canada’s Food
and Drugs Act and Natural Health Product Regulations.
This means obtaining various approvals from Health Canada,
the Canadian regulatory authority, before doing so. The two main
approvals required to import and sell NHPs in
Canada
are: (1) a Product License; and (2) a Site License.
Where a product is considered to be a
“drug,” similar, but more much more onerous approval and
licensing requirements apply.
Product
License
Obtaining a Product License involves
submitting an application to Health Canada with evidence of the
NHP’s safety, efficacy, and quality.
This can be an onerous process and may include submitting
clinical test data or studies from the scientific literature to
Health Canada for assessment.
However, in some cases where a product’s safety and
efficacy are already well-established (e.g. calcium, Echinacea),
it may be possible to base the NHP application on a
“monograph” for that product, providing a quicker route for
NHP approval.
If Health Canada approves an NHP, it will
issue a Product License for that product.
Until an NHP is approved and issued a Product License,
claims made in advertising
or marketing the NHP are unverified and may be considered
misleading or deceptive.
At
present time, there is a very long waiting list for Product
Licenses, and most new entrants to the market-place attempt to
enter the market on the basis of a “submission number”
provided by Health Canada on receipt of a complete Product License
application.
Note, however, that even where “submission
numbers” are obtained, the Canada Border Services Agency will
still require a valid “Site License” (see below) before
allowing commercial shipments of NHPs across the Canadian border.
Site
Licenses
Apart from the requirement to have a Product
License, any company importing an NHP for sale in Canada must hold
a “Site License” before the Canada Border Services Agency will
allow commercial shipments of NHPs across the Canadian border.
As foreign companies cannot apply for a Site
License, they may wish to import through a Canadian subsidiary, or
engage another company, such as a broker or logistics company,
holding a valid Site License, in order to import.
An
Alternative Way to Sell to Canadians
Faced with the fairly daunting requirements
for entering the Canadian market-place, and an untested Canadian
market, some non-resident vendors seek an alternative means to
sell NHPs to Canadians.
One currently available option is to
structure sales to Canadians around Health Canada’s personal use
importation policy (the “Personal Importation Policy”).
Generally speaking, the Personal Importation Policy allows
individual Canadians to import unapproved NHPs for
personal use, but not for commercial or other distribution.
If the Personal Importation Policy applies,
then the NHP does not require a Product License and the individual
importing the NHP does not require a Site License.
However,
there are important limitations to the Personal Importation
Policy, which must be taken into account of in structuring the
non-resident company’s sales policies, and sales agreement with
any Canadian customers.
Further,
the Personal Importation Policy
will not apply to all health products, as certain drug ingredients
are subject to specific import restrictions and cannot be imported
under the Personal Importation Policy.
Accordingly,
with the proper structuring and limitations, it is often possible
for a non-resident to sell to Canadians, yet without coming under
the jurisdiction and control of the Canadian Food
and Drugs Act..
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Feel
free to contact a lawyer at
MILLAR
KREKLEWETZ LLP who can
consult and advise you on
Food
and Drugs Act matters.
Feel free to contact us for a no cost initial
consultation.
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Kreklewetz LLP
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