< > W380 - Food and Drug Administration, U.S. Department of Health and Human Services - http://www.fda.gov

General Information

Please note:

  • This hyperlink was operational at time of referencing this website.
  • The hyperlink will only work when you are "on-line".
  • Information on the Internet changes frequently and this reference relates only to the data drawn down from the internet on the date in the reference suffix (e.g. W1.May00)
Organisation Reference Food and Drug Administration (FDA), U.S. Department of Health and Human Services 
Wildpro Referenced Responsibilities:- Conventions, Legislation, Codes of Conduct, Manuals --

This web-link has been created as part of the "Managing for West Nile Virus Infection in the USA" Wildpro module. Consult the Specific Section References at the end of this page for related links. 

Notes

This information has been taken directly from the FDA Website:

"Stated most simply, FDA's mission is to promote and protect the public health by helping safe and effective products reach the market in a timely way, and monitoring products for continued safety after they are in use. Our work is a blending of law and science aimed at protecting consumers."

"FDA is the federal agency responsible for ensuring that foods are safe, wholesome and sanitary; human and veterinary drugs, biological products, and medical devices are safe and effective; cosmetics are safe; and electronic products that emit radiation are safe. FDA also ensures that these products are honestly, accurately and informatively represented to the public."

"Some of the agency's specific responsibilities include:

Biologics:

  • product and manufacturing establishment licensing
  • safety of the nation's blood supply
  • research to establish product standards and develop improved testing methods
Cosmetics:
  • labeling
  • adverse reactions
  • alpha hydroxy acids
Drugs:
  • product approvals
  • OTC and prescription drug labeling
  • drug manufacturing standards
Electronic Products:
  • radiation safety performance standards for microwave ovens, cell phones, television receivers, diagnostic x-ray equipment, cabinet x-ray systems (such as baggage x-rays at airports), laser products, ultrasonic therapy equipment, mercury vapor lamps, and sunlamps
  • accrediting and inspecting mammography facilities
Foods:
  • labeling
  • safety of all food products (except meat and poultry)
  • bottled water

Medical Devices:

  • premarket approval of new devices
  • manufacturing and performance standards
  • tracking reports of device malfunctioning and serious adverse reactions
Veterinary Products:
  • livestock feeds
  • pet foods
  • veterinary drugs and devices

When Does FDA Get Involved?

FDA has legal jurisdiction over products shipped in interstate commerce. A product that is manufactured, shipped and marketed within a state is not, in most cases, subject to FDA regulation. Often, states will adopt guidelines, and they are responsible for ensuring compliance. Consumers with questions or complaints about products that are not involved in interstate commerce should contact their state governments.

Individual states are also responsible for licensing and monitoring the conduct of physicians, pharmacists, and other health-care professionals. State and local governments are also responsible for the inspection and regulation of establishments such as restaurants and health spas."

Further information on the FDA Center for Veterinary Medicine (CVM)

The Center for Veterinary Medicine (CVM) regulates the manufacture and distribution of food additives and drugs that will be given to animals. These include animals from which human foods are derived, as well as food additives and drugs for pet (or companion) animals. CVM is responsible for regulating drugs, devices, and food additives given to, or used on, over one hundred million companion animals, plus millions of poultry, cattle, swine, and minor animal species. (Minor animal species include animals other than cattle, swine, chickens, turkeys, horses, dogs, and cats.)

The Center for Veterinary Medicine is a consumer protection organization. We foster public and animal health by approving safe and effective products for animals and by enforcing applicable provisions of the Federal Food, Drug, and Cosmetic Act and other authorities. 

The Food and Drug Administration's Center for Veterinary Medicine (CVM) is responsible for assuring that animal drugs and medicated feeds are safe and effective and that food from treated animals is safe to eat. This authority is derived from the Federal Food, Drug, and Cosmetic Act (the Act). The Act was amended in 1968 to include sections which specifically address animal drugs. These amendments were designed to ensure that animal drugs are safe and effective for their intended uses and that they do not result in unsafe residues in foods. 

One of CVM's highest priorities is assuring the safety of the food supply. And, because of the Center's work and the cooperative efforts of all FDA employees, the American food supply is among the safest in the world. 

The responsibilities of CVM have a direct effect on the safety of the human food supply and on the safety to animals of veterinary products. 

CVM works to educate consumers as well as the regulated industry; evaluates data on proposed veterinary products carefully before permitting them to be marketed; discovers volatile marketed products through surveillance programs, and initiates legal action, if necessary, to bring violators into compliance with the law; and conducts research to support Center activities. 

Whether developing and disseminating information, approving animal drug products for marketing, monitoring marketed animal drug products, or conducting research, CVM is committed to the important goal of protecting animal and human health throughout the United States. 

Mission Statement

The Center for Veterinary Medicine is a consumer protection organization. We foster public and animal health by approving safe and effective products for animals and by enforcing other applicable provisions of the Federal Food, Drug, and Cosmetic Act and other authorities. 

Vision Statement
We are an internationally recognized public health organization responsible for the evaluation, approval and/or surveillance of animal drugs, food additives, feed ingredients, and animal devices. We are proactive in our efforts to increase the availability and diversity of safe and effective products that relieve animal pain and suffering, sustain their health, improve animal productivity and do not compromise public health. We adapt, align and utilize our resources wisely and make practical use of state of the art science and technologies to best accomplish our mission. People with expertise in product evaluation, research, surveillance, compliance and other functional areas work cooperatively as an integrated team. We foster open and collegial partnerships with our constituencies to respond to concerns and needs. We maintain a worker-friendly environment, foster initiatives, and value cultural diversity and nourish individual growth and professional development. Everyone exhibits pride in the organization, values and recognizes the contribution and accomplishments of each member of the CVM team, and demonstrates mutual trust and respect. The entire Center pulls in the same direction with purpose, harmony, and grace. We all live by, and our managers exemplify the Center's guiding principles. By recognizing the expertise of everyone, we inspire cooperative decision-making. All are empowered to participate in the development of policy as well as to take responsibility for making decisions within those policy boundaries.

Dates Referenced December 2002, June 2004
Contact Details FDA-CVM:

Food and Drug Administration
Center for Veterinary Medicine
Communications Staff
7519 Standish Place, HFV-12
Rockville, Maryland 20855
301-827-3800

[For paper copies of guidance documents, CVM Updates, CVM Memos, information fliers, and other documents posted on the Home Page]

Website Address

www.fda.gov

Email

Return to top of page

Specific References (Please note - website addresses change frequently and all references are dated accordingly. If hyperlinks are no longer active, please inform us)

Reference Section of Website Specific Website link
W380.Dec02.wnv1 Guidance for Industry: Recommendations for the Assessment of Donor Suitability and Blood and Blood Product Safety in Cases of Known or Suspected West Nile Virus Infection www.fda.gov/cber/gdlns/wnvguid.htm

www.fda.gov/cber/gdlns/wnvguid.pdf

W380.24Mar03.CWD1 FOOD AND DRUG ADMINISTRATION ACTION PLAN TRANSMISSIBLE SPONGIFORM ENCEPHALOPATHIES including Bovine Spongiform Encephalopathy
And Chronic Wasting Disease 24 APRIL 2001
http://www.fda.gov/oc/oca/roundtable/bse/FDA_actionplan.html
W380.24Mar03.CWD2 CVM Update November 12, 2002MATERIAL FROM CWD-POSITIVE ANIMALS SHOULD NOT BE USED FOR ANIMAL FEED www.fda.gov.cvm/index/updates/Cwdup.htm

 

W380.29Jun03.CWD1 Draft Issue Summaries, Background Document Chronic Wasting Disease http://www.fda.gov/ohrms/dockets/ac/01/briefing/3681b1_03.doc
W380.29Jun03.CWD2 FDA Talk Paper T03-34, May 15, 2003, FDA Issues Draft Guidance on Use of Material From Deer and Elk in Animal Feed http://www.fda.gov/bbs/topics/ANSWERS/2003/ANS01220.html
W380.29Jun03.CWD3 Guidance for Industry - Use of Material from Deer and Elk in Animal Feed: DRAFT GUIDANCE http://www.fda.gov/cvm/guidance/dguide158.pdf

Return to top of page