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Is
this regulation not about quality control of herbal medicine?
That is what the pro regulation lobby are trying to make you think.
In reality we have two distinctly different issues which they
are trying to interweave to fool you.
1. Regulations
on the quality and available of herbal preparations:
a)
Regulation of the quality of manufactured Herbal preparations
has been an ongoing process for some years. Herbal manufacturers
already have to submit to some stringent regulations on quality
control and on ingredients. Quality control of manufactured remedies
is fine as is quality control of herbs imported from far flung
countries. However, the detailed checking of such imports is rarely
enforced at the points of entry as was shown up a couple of years
ago over contaminated herbal powders used in foods. That is an
aspect that badly needs tightening up, but of course that costs
the Government money!
It is contaminated
herbal imports that gave the MHRA the ammunition they needed to
draft their regulations. These were products which UK traditional
herbalists did not use. In the days when most herbal medicine
in the UK was our own traditional system, the herb importers had
the highest expertise in quality control. They knew where the
herbs they imported came from and had a detailed knowledge of
what to be on the lookout for, including chemical and microscopic
testing.
b) Control
on the quality of herbs gathered in the wild in the UK, or grown
and prescribed by a traditional practitioner with thousands of
years of knowledge to draw on is another thing. Do we really want
to be told what hedgerow we can't gather from, or that the overworked
understaffed Environmental Health departments must monitor what
is picked and prescribed?
2. Regulation
of the practitioners:
This
is an issue that it is claimed is being forced on us by European
legislation. However, no one has checked if that legislation may
not be applicable to the UK, under the treaties which our government
signed.
The pro regulation
lobby intentionally confuse the two issues by constantly
referring to the European policy documents which have nothing
to do with practitioner registration such as the 'Traditional
Herbal Medicinal Products Directive (2004/24/EC)'. As with practitioner
regulation, it is open to debate as to if the EU Directives can
legally be forced on the UK due to our traditional systems enshrined
in existing legislation. This clause in the Treaty of Rome is
key to this:
2.
"The Union shall respect fundamental rights, as guaranteed
by the European Convention for the Protection of Human Rights
and Fundamental Freedoms signed in Rome on 4 November 1950 and
as they result from the CONSTITUTIONAL TRADITIONS
common to the Member States, as general principles of Community
law".
Article
3.
(o) a contribution
to the attainment of a high level of health protection;
(p) a contribution
to education and training of quality and to the FLOWERING OF THE
CULTURES of the Member States;
In the UK,
freedom of health care provision is part of our cultural identity.
Therefore any activity that threatens that is suppressing not
supporting the flowering of the cultures.
There are
several other clauses in these fundamental Treaties that set up
the European Community that may affect our unique traditional
legislation over herbalists. The huge problem with the EU is that
they appoint unrepresentative advisory committee's (often without
real experts on what they are examining), who then draft regulations
without any input from the trades they will affect. The European
Commission is an anti democratic organisation that does not
even comply with its own constitution, yet the UK Government seems
happy to simply slip into existence their badly drafted laws without
proper Parliamentary scrutiny. Our laws are now being drafted
and discussed in the EU by non expert committees with little if
any input from the sectors of society that their recommendations
will affect. Please see the Cropwatch
web site for some great examples of the way the EU committees
work.
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