
Canadian Bill C51 purportedly proposes sweeping changes to the herbal supplement and naturopathic/homeopathic remedies market. The following excerpted from an anti Bill C51 website, although not independently confirmed, suggests that the bill would (amongst other things):
1) Fasttrack pharmaceutical drug approval and
2) Make over 70% percent of current herbal drugs illegal.
Now, this was taken from an opposing website so all claims must then be taken with a grain of all natural sea salt. The Government claims that your access to Vitamin C and Echinacea is safe.
“Under Bill C-51, Canadians will continue to have access to natural health products that are safe, effective and of high quality. The Bill will not limit access to natural health products nor does it call for a change in their regulatory status (from over-the-counter to prescription)” says Health Canada spokesperson Paul Duchesne.
Source :: http://www.ctv.ca/servlet/ArticleNews/story/CTVNews/20080509/C51_protests_080509/20080510?hub=TopStories
From that simple quote we are forced to ask the question, who and how will products be determined to be ‘safe, effective and of high quality’? The contention seems to be over semantics and the definition of exactly which products will and will not be regulated. Putting semantic issues aside, it looks as though the combatants are missing the more global issue and that is in addressing the manner in which the allopathic (mainstream) and alternative medicine operate. The issue is probably more complex than first fathomed. Both paradigms operate under different modi operandorum.
Big pharma operates under the model of providing drugs and therapies with validated claims. The drug’s claims and safety are established by clinical drug trials. The benefits here should be obvious but the weaknesses of this system may not be. The first failure of the big pharma model is that drug trials can be flawed either intentionally or just by simple lack of scope or experimental design. Take for example the drug VIOXX which did pass clinical trials and FDA approval which was later associated with heart disease and voluntarily withdrawn by its manufacturer Merck. http://en.wikipedia.org/wiki/Rofecoxib#Withdrawal The second failing of the big pharma model is even more subtle in that only patentable therapies need apply. Take for example the research Dr. Evangelos Michelak out of the university of Alberta who has come up with a cancer treatment using the chemical DCA. http://www.depmed.ualberta.ca/dca/ This treatment has been conclusively shown to remove or eradicate all manner of cancers in test animals. It is a hugely promising therapy with suprisingly few side effects. One would expect this drug to be in human trial by now. However, since DCA is not patentable, (almost as common as table salt) the drug companies have no interest. DCA will go to human trial nonetheless, but only after Dr. Evangelos Michelak is able to scrape together enough money from other philanthropic investors.
Now let’s examine the world of home or natural remedies. You can pick up a bottle of an herbal remedy which can make all manner of claims. These claims need not be validated and, indeed, the only validation you’ll receive is either from the smiling face of the salesperson at your natural foods store or the recommendation of a friend or naturopatic practitioner. However, you probably won’t be able to rely on any study and you’ll have to adopt a ‘take it and try it’ approach. The failings of this system are two fold. First, hearkening back to the days of the snake oil salesmen, there is the potential for you to waste your time and money on ineffective remedies. Second, in wasting your time on these remedies, you may delay seeking appropriate medical treatment for a potentially serious condition. The first failure – the lack of study based findings — is compelling. The natural health product industry needs to provide better support for their claims and adhere to some standard as for quality of composition. The second failure is not as compelling as people typically resort to natural health products only after the failure or reticence of allopathic medicine.
Looking at both paradigms, there is a measure which could marry their strengths and divorce ourselves of their weaknesses. The summary of bill C51 reads as follows:
This enactment amends the Food and Drugs Act to modernize the regulatory system for foods and therapeutic products, to strengthen the oversight of the benefits and risks of therapeutic products throughout their life cycle, to support effective compliance and enforcement actions and to enable a greater transparency and openness of the regulatory system.
Source :: http://www2.parl.gc.ca/HousePublications/Publication.aspx?DocId=3398126&File=19
If this is indeed the goal of the Federal Government, then wouldn’t their time and efforts be better spent in implementing a system of subsidized and facilitated human trials? A subsidized and facilitated human trials system would raise the bar for natural health food products to better support their claims. Since the studies would be subsidized and facilitated we wouldn’t deny ourselves access to any reasonable therapy but as consumers, claims of product effectiveness and quality of composition could be properly backed by more than a friendly smile. All therapies, herbal and pharmaceutical would be subject to the same level of testing. This testing would be reasonably affordable for any given company. This would satisfy the allopathic community’s demands for rigorous proof and testing while at the same time allow the allopathic community to consider previously unprofitable yet promising treatments such as DCA.
There is a petition circulating to stop bill C51. http://www.thepetitionsite.com/1/StopC51 I would be willing to sign it if it could be proved it would make 70% of current natural health care products illegal. Would I sign a petition to have the Federal Government fund and facilitate human trials of all health care products? In a heartbeat.