Control of Homeopathy - Was: Homeopathic pharmacy responsibilities
Posted: Thu May 28, 2009 3:26 pm
Again, I have not been able to read a lot of what went on before but it seems to me that there is not much time left in which pharmacies and homeopaths will be able to do what they like with their remedies.
Things are being moved into place to control homeopathy and the production of its medicines. It is more advanced in some countries than in others but will probably soon be global as a result of the push for 'harmonisation'.
For example, the access and use of nosodes is becoming more and more restrictive. If what is happening in Australia is representative of what will happen elsewhere (and in some countries it is even more advanced), drug regulating authorities will take greater control of the regulation of homeopathic medicines, especially the nosodes.
These remedies - produced from animal or human origin - will quite probably not be allowed to be sold or distributed in the future until they meet the safety requirements of those agencies - prions from the mad cow problem will be cited as one of the reason for this, and the need to ensure good manufacturing practices. This is what currently exists in Australian legislation and last time I checked quite a few years ago, assessment and approval by our agency would cost near to $100,000 for each remedy. Currently, changes are underway that will lead to the introduction of even more onerous legislation. From what I understand, the same is underway in many other countries.
In the future, it is quite probable that a paper trail of each remedy, nosodes especially, will be required stating the source of the original substance, how and when it was collected and transported, which pharmacy was responsible for its preparation and under what conditions, and to whom the remedy was subsequently supplied. When you consider that we have no idea about the source, the when, and the how of many of our nosodes, it is easy to see that in one fell swoop there is the potential to lose many of our remedies.
We will also have to justify the reasons for their use so quite possibly reprovings will have to be done, especially for remedies with which there are mainly clinical indications. For those nosodes that have no provings - most of them, we could lose the right to produce, purchase and use them altogether.
In a post someone recently placed on another list they told of how 8 FDA agents raided Homeopathy Works in the states regarding nosodes early in April this year. Does anyone know anything further about this?
david hartley wrote:
--
Kind regards,
Fran Sheffield
Homeopathy Plus! (Tutorials - Remedies - Immunisation)
http://www.homeopathyplus.com.au
Do No Harm Initiative (Free Information on Homeopathic Immunisation)
http://www.d-n-h.org
Homeopathy for Autism (Guidelines for Treatment - Search for Practitioners)
http://www.homeopathy4autism.com
Things are being moved into place to control homeopathy and the production of its medicines. It is more advanced in some countries than in others but will probably soon be global as a result of the push for 'harmonisation'.
For example, the access and use of nosodes is becoming more and more restrictive. If what is happening in Australia is representative of what will happen elsewhere (and in some countries it is even more advanced), drug regulating authorities will take greater control of the regulation of homeopathic medicines, especially the nosodes.
These remedies - produced from animal or human origin - will quite probably not be allowed to be sold or distributed in the future until they meet the safety requirements of those agencies - prions from the mad cow problem will be cited as one of the reason for this, and the need to ensure good manufacturing practices. This is what currently exists in Australian legislation and last time I checked quite a few years ago, assessment and approval by our agency would cost near to $100,000 for each remedy. Currently, changes are underway that will lead to the introduction of even more onerous legislation. From what I understand, the same is underway in many other countries.
In the future, it is quite probable that a paper trail of each remedy, nosodes especially, will be required stating the source of the original substance, how and when it was collected and transported, which pharmacy was responsible for its preparation and under what conditions, and to whom the remedy was subsequently supplied. When you consider that we have no idea about the source, the when, and the how of many of our nosodes, it is easy to see that in one fell swoop there is the potential to lose many of our remedies.
We will also have to justify the reasons for their use so quite possibly reprovings will have to be done, especially for remedies with which there are mainly clinical indications. For those nosodes that have no provings - most of them, we could lose the right to produce, purchase and use them altogether.
In a post someone recently placed on another list they told of how 8 FDA agents raided Homeopathy Works in the states regarding nosodes early in April this year. Does anyone know anything further about this?
david hartley wrote:
--
Kind regards,
Fran Sheffield
Homeopathy Plus! (Tutorials - Remedies - Immunisation)
http://www.homeopathyplus.com.au
Do No Harm Initiative (Free Information on Homeopathic Immunisation)
http://www.d-n-h.org
Homeopathy for Autism (Guidelines for Treatment - Search for Practitioners)
http://www.homeopathy4autism.com