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Human Medications, Human Drugs, Animal Medications, Animal Drugs, Pharmacy law, Pharmaceutical law, Compounding law, Sterile and Non Sterile Compounding 797 Compliance, Veterinary law, Veterinary Compounding Law; Health Care; Awareness of all Types of Compounding Issues; Pharmacy Benefit Managers (PBMs), Outsourcing Facilities Food and Drug Administration and Compliance Issues
Showing posts with label Veterinary Drug Compounding. Show all posts
Showing posts with label Veterinary Drug Compounding. Show all posts
Tuesday, February 12, 2013
Tuesday, April 17, 2012
FDA Division of Compliance: Inspecting Businesses that May be Manufacturing Under Guise of Compounding
The Division of Compliance of the United States Food and Drug Administration (FDA) has issued assignments to conduct inspections of firms, including internet pharmacies, who may be engaged in the practice of manufacturing under the guise of pharmacy compounding. The FDA web site contains the following statement regarding Veterinary Drug Compounding.
Preapproval inspections are conducted pursuant to pending NADA or ANADA applications.
Inspections, Compliance, and Criminal Investigations
.9.2 - VETERINARY DRUG ACTIVITIES
CVM is responsible for inspections of therapeutic and production drugs, and Active Pharmaceutical Ingredients (APIs). Therapeutic drugs are used in the diagnosis, cure, mitigation, treatment or prevention of disease. Production drugs are used for economic enhancement of animal productivity. Examples include: growth promotion, feed efficiency and increased milk production.Preapproval inspections are conducted pursuant to pending NADA or ANADA applications.
Post approval inspections of veterinary drugs are
conducted to determine compliance with the Current Good Manufacturing Practices
(CGMPs) for Finished Pharmaceuticals under 21
CFR Part 2113. These cGMPs
apply to both human and veterinary drugs. Information on veterinary drugs
approved can be found in the "Green Book" database accessed through CVM's
website.
APIs are active pharmaceutical ingredients. Many of the APIs used to
manufacture dosage form drugs are imported from foreign countries. The intended
source for an API must be indicated in NADA/ANADA submissions for new animal
drug approvals. Any change in a source for an API would require a supplement to
the application.
Extra label drug use refers to the regulations in 21
CFR Part 5304 codified as a
result of the Animal Medicinal Drug Use Clarification Act5 (AMDUCA) of 1994. These regulations
set forth the requirements that veterinarians must meet to prescribe extra label
uses of FDA approved animal and human drugs. The regulations describe what is a
valid veterinary-client-patient relationship as well as what is considered
illegal extra label use. 21 CFR Part 530 addresses issues regarding extra label
use in non-food as well as food producing animals. 21
CFR 530.416 contains a list of
drugs that cannot be used in an extra label manner in food-producing animals.
During an inspection or investigation if you encounter any situations on
suspected illegal extra label use of any FDA approved animal or human drugs or
those prohibited for extra label use in food animals, you should contact CVM's
Division of Compliance (HFV-230) (240-276-9200).
21 CFR Part 530 also addresses compounding of
products from approved animal or human drugs by a pharmacist or veterinarian.
The regulations clearly state compounding is not permitted from bulk drugs. This
would include APIs. CVM has an existing CPG on Compounding of Drugs for Use in
Animals (CPG 608.4007). A
copy can be found on CVM's website. The Division of Compliance (HFV-230) has
issued assignments to conduct inspections of firms, including internet
pharmacies, who may be engaged in the practice of manufacturing under the guise
of pharmacy compounding. You should contact the Division of Compliance (HFV-230)
at 240-276-9200 to report instances of compounding or to seek guidance on
inspectional issues, or regulatory and enforcement policies.
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