Scope of the Public Hearing; Homeopathic Product Regulation
Posted: Sat Apr 04, 2015 9:21 pm
Hi all,
http://medical-dictionary.thefreedictionary.com/drug
"drug
(drug)
1. a chemical substance that affects the processes of the mind or body.
2. any chemical compound used in the diagnosis, treatment, or prevention of disease or other abnormal condition.
3. a substance used recreationally for its effects on the central nervous system, such as a narcotic.
4. to administer a drug to."
-------------------------------
http://www.fda.gov/AboutFDA/Transparenc ... 194516.htm
"What is a biological product?
Biological products, or biologics, are medical products. Many biologics are made from a variety of natural sources (human, animal or microorganism). Like drugs, some biologics are intended to treat diseases and medical conditions. Other biologics are used to prevent or diagnose diseases. Examples of biological products include
vaccines
blood and blood products for transfusion and/or manufacturing into other products
allergenic extracts, which are used for both diagnosis and treatment (for example, allergy shots)
human cells and tissues used for transplantation (for example, tendons, ligaments and bone)
gene therapies
cellular therapies
tests to screen potential blood donors for infectious agents such as HIV"
---------------------------------
http://www.regulations.gov/#!documentDe ... -0540-0001
"Scope of the Public Hearing
FDA is seeking broad public input on the current enforcement policies related to drug products labeled as homeopathic in an effort to better promote and protect the public health. FDA has developed a list of questions to facilitate a more productive discussion at the public hearing. This list is not intended to be exclusive, and FDA encourages comments on other matters related to the development and regulation of drug and biological products labeled as homeopathic. Issues that are of specific interest to the Agency include the following:
What are consumer and health care provider attitudes towards human drug and biological products labeled as homeopathic?
What data sources can be identified or shared with FDA so that the Agency can better assess the risks and benefits of drug and biological products labeled as homeopathic?
Are the current enforcement policies under the CPG appropriate to protect and promote public health in light of the tremendous growth in thehomeopathic drug market? Are there alternatives to the current enforcement policies of the CPG that would inform FDA's regulatory oversight of drugs labeled as homeopathic? If so, please explain.
Are there areas of the current CPG that could benefit from additional clarity? If so, please explain.
Is there information regarding the regulation of homeopathic products in other countries that could inform FDA's thinking in this area?
A large majority of human drug products labeled as homeopathic are marketed as OTC drugs. These products are available for a wide variety of indications, and many of these indications have never been considered for OTC use under a formal regulatory process. What would be an appropriate regulatory process for evaluating such indications for OTC use?
Given the wide range of indications on drug products labeled as homeopathic and available OTC, what processes do companies currently use to evaluate whether such products, including their indications for use, are appropriate for marketing as an OTC drug?
Do consumers and health care providers have adequate information to make informed decisions about drug products labeled as homeopathic? If not, what information, including, for example, information in labeling, would allow consumers and health care providers to be better informed about products labeled as homeopathic?"
Atb,
Leilanae
http://medical-dictionary.thefreedictionary.com/drug
"drug
(drug)
1. a chemical substance that affects the processes of the mind or body.
2. any chemical compound used in the diagnosis, treatment, or prevention of disease or other abnormal condition.
3. a substance used recreationally for its effects on the central nervous system, such as a narcotic.
4. to administer a drug to."
-------------------------------
http://www.fda.gov/AboutFDA/Transparenc ... 194516.htm
"What is a biological product?
Biological products, or biologics, are medical products. Many biologics are made from a variety of natural sources (human, animal or microorganism). Like drugs, some biologics are intended to treat diseases and medical conditions. Other biologics are used to prevent or diagnose diseases. Examples of biological products include
vaccines
blood and blood products for transfusion and/or manufacturing into other products
allergenic extracts, which are used for both diagnosis and treatment (for example, allergy shots)
human cells and tissues used for transplantation (for example, tendons, ligaments and bone)
gene therapies
cellular therapies
tests to screen potential blood donors for infectious agents such as HIV"
---------------------------------
http://www.regulations.gov/#!documentDe ... -0540-0001
"Scope of the Public Hearing
FDA is seeking broad public input on the current enforcement policies related to drug products labeled as homeopathic in an effort to better promote and protect the public health. FDA has developed a list of questions to facilitate a more productive discussion at the public hearing. This list is not intended to be exclusive, and FDA encourages comments on other matters related to the development and regulation of drug and biological products labeled as homeopathic. Issues that are of specific interest to the Agency include the following:
What are consumer and health care provider attitudes towards human drug and biological products labeled as homeopathic?
What data sources can be identified or shared with FDA so that the Agency can better assess the risks and benefits of drug and biological products labeled as homeopathic?
Are the current enforcement policies under the CPG appropriate to protect and promote public health in light of the tremendous growth in thehomeopathic drug market? Are there alternatives to the current enforcement policies of the CPG that would inform FDA's regulatory oversight of drugs labeled as homeopathic? If so, please explain.
Are there areas of the current CPG that could benefit from additional clarity? If so, please explain.
Is there information regarding the regulation of homeopathic products in other countries that could inform FDA's thinking in this area?
A large majority of human drug products labeled as homeopathic are marketed as OTC drugs. These products are available for a wide variety of indications, and many of these indications have never been considered for OTC use under a formal regulatory process. What would be an appropriate regulatory process for evaluating such indications for OTC use?
Given the wide range of indications on drug products labeled as homeopathic and available OTC, what processes do companies currently use to evaluate whether such products, including their indications for use, are appropriate for marketing as an OTC drug?
Do consumers and health care providers have adequate information to make informed decisions about drug products labeled as homeopathic? If not, what information, including, for example, information in labeling, would allow consumers and health care providers to be better informed about products labeled as homeopathic?"
Atb,
Leilanae