This can't be too good. They have probably figured out that those who do not vaccinate rely on homeopathy and looking for pretext to make remedies less readily available. Sure there is always Helios, but if FDA starts regulating it, then what?
Victoria
FDA PUBLIC HEARING ABOUT HOMEOPATHICS
View this email in your browser
FYI: THIS JUST ARRIVED FROM THE FDA
Dear Colleague,
FDA is announcing a public hearing to obtain information and comments from stakeholders about the current use of human drug and biological products labeled as homeopathic, as well as the Agency’s regulatory framework for such products. These products include prescription drugs and biological products labeled as homeopathic and over-the-counter (OTC) drugs labeled as homeopathic. FDA is seeking participants for the public hearing and written comments from all interested parties, including, but not limited to, consumers, patients, caregivers, health care professionals, patient groups, and industry. FDA is seeking input on a number of specific questions, but is interested in any other pertinent information participants would like to share.
For more information:
* Review the Federal Register notice
* Visit the FDA website on the topic
Regards,
Shannon Thor, PharmD
Health Programs Coordinator
Office of Health & Constituent Affairs
Office of External Affairs
U.S. Food and Drug Administration
Tel: 301.796.8645
Shannon.Thor@fda.hhs.gov
MOnday meeting Agenda
Re: MOnday meeting Agenda
Although it would be nice to stop the use of “homeopathic” labels for those combo remedies like stress tabs that are in a mint base, for example. Not homeopathic, just potentized ingredients.
Sherill
From: minutus@yahoogroups.com [mailto:minutus@yahoogroups.com]
Sent: Thursday, March 26, 2015 9:53 PM
To: minutus@yahoogroups.com
Subject: [Minutus] Fwd: FW: MOnday meeting Agenda
This can't be too good. They have probably figured out that those who do not vaccinate rely on homeopathy and looking for pretext to make remedies less readily available. Sure there is always Helios, but if FDA starts regulating it, then what?
Victoria
FDA PUBLIC HEARING ABOUT HOMEOPATHICS
View this email in your browser
FYI: THIS JUST ARRIVED FROM THE FDA
Dear Colleague,
FDA is announcing a public hearing to obtain information and comments from stakeholders about the current use of human drug and biological products labeled as homeopathic, as well as the Agency’s regulatory framework for such products. These products include prescription drugs and biological products labeled as homeopathic and over-the-counter (OTC) drugs labeled as homeopathic. FDA is seeking participants for the public hearing and written comments from all interested parties, including, but not limited to, consumers, patients, caregivers, health care professionals, patient groups, and industry. FDA is seeking input on a number of specific questions, but is interested in any other pertinent information participants would like to share.
For more information:
* Review the Federal Register notice
* Visit the FDA website on the topic
Regards,
Shannon Thor, PharmD
Health Programs Coordinator
Office of Health & Constituent Affairs
Office of External Affairs
U.S. Food and Drug Administration
Tel: 301.796.8645
Shannon.Thor@fda.hhs.gov
Sherill
From: minutus@yahoogroups.com [mailto:minutus@yahoogroups.com]
Sent: Thursday, March 26, 2015 9:53 PM
To: minutus@yahoogroups.com
Subject: [Minutus] Fwd: FW: MOnday meeting Agenda
This can't be too good. They have probably figured out that those who do not vaccinate rely on homeopathy and looking for pretext to make remedies less readily available. Sure there is always Helios, but if FDA starts regulating it, then what?
Victoria
FDA PUBLIC HEARING ABOUT HOMEOPATHICS
View this email in your browser
FYI: THIS JUST ARRIVED FROM THE FDA
Dear Colleague,
FDA is announcing a public hearing to obtain information and comments from stakeholders about the current use of human drug and biological products labeled as homeopathic, as well as the Agency’s regulatory framework for such products. These products include prescription drugs and biological products labeled as homeopathic and over-the-counter (OTC) drugs labeled as homeopathic. FDA is seeking participants for the public hearing and written comments from all interested parties, including, but not limited to, consumers, patients, caregivers, health care professionals, patient groups, and industry. FDA is seeking input on a number of specific questions, but is interested in any other pertinent information participants would like to share.
For more information:
* Review the Federal Register notice
* Visit the FDA website on the topic
Regards,
Shannon Thor, PharmD
Health Programs Coordinator
Office of Health & Constituent Affairs
Office of External Affairs
U.S. Food and Drug Administration
Tel: 301.796.8645
Shannon.Thor@fda.hhs.gov
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- Posts: 394
- Joined: Thu Mar 20, 2014 11:00 pm
Re: MOnday meeting Agenda
Victoria: I think this may also have something to do with the TOP SECRET TPP trade agreement. Obama's trying to get the US Congress to give him Fast Track authority to negotiate for CORPORATE AMERICA. If my hunch is right and it is about TPP, then it's BIG PHARMA and the other multinationals going after a bigger share of the profits!
Call your congressional delegations and put in your "ask" for a NO on TPP Fast Track.
Vicki
Call your congressional delegations and put in your "ask" for a NO on TPP Fast Track.
Vicki