Guidance for Industry
Possible Dioxin/PCB Contamination of Drug and Biological Products
[PDF version]
Additional copies of this guidance document are available from:
Office of Training and Communications
Division of Communications Management
Drug Information Branch, HFD-210
Center for Drug Evaluation and Research
Food and Drug Administration
5600 Fishers Lane, Rockville, MD 20857
(Phone 301-827-4573)
Internet: http://www.fda.gov/cder/guidance/index.htm
or
Office of Communication, Training and Manufacturers Assistance, (HFM-40)
Center for Biologics Evaluation and Research (CBER)
Food and Drug Administration
1401 Rockville Pike, Rockville, MD 20852-1448
(Internet) http://www.fda.gov/cber/guidelines.htm
Phone: The Voice Information System at 800-835-4709 or 301-827-1800
or
Communications Staff (HFV-12)
Center for Veterinary Medicine (CVM)
7500 Standish Place, Rockville, MD 20855
(Tel) 301-594-1755
http://www.fda.gov/cvm
U.S. Department of Health and Human Services
Food and Drug Administration
Center for Drug Evaluation and Research (CDER)
Center for Biologics Evaluation and Research (CBER)
Center for Veterinary Medicine (CVM)
August 1999
Compliance
Guidance for Industry1
Possible Dioxin/PCB Contamination of Drug and Biological Products
| This guidance represents the Agency's current thinking on possible dioxin/PCB contamination of animal source material in EU countries. It does not create or confer any rights for or on any person and does not operate to bind FDA or the public. An alternative approach may be used if such approach satisfies the requirements of the applicable statutes, regulations, or both. |
- INTRODUCTION
This guidance is intended for manufacturers using materials derived from animal sources in the manufacture of human or animal drugs or biological products. During the period from January through June 1999, some poultry, swine, and ruminants (cattle, sheep, and goats) in several EU (European Union) countries were fed feed contaminated with dioxins and PCBs (polychlorinated biphenyls). As a result, animals that received the contaminated feed became contaminated with dioxins and PCBs. Manufacturers who are using materials from such animal sources in the manufacture of their products should verify that the materials they are using are not from animals affected during the contamination incident, or conduct suitable testing of the materials.
- RECOMMENDATIONS FOR ASSESSING ANIMAL DERIVED MATERIALS
Because of the potential contamination of animals in Belgium, France, and the Netherlands, manufacturers should investigate the origin of animal derived materials (e.g. egg yolk lecithin, egg phospholipids, pancrelipase) they are using to manufacture human or animal drugs or biological products. This includes drug substances and excipients. If materials are found to be derived from poultry, swine, or ruminants, manufacturers should obtain certification from their suppliers that the animal derived materials (including the eggs from chickens) used in drugs or biological product manufacturing do not come from animals raised in any of these three countries during the period January through June 1999. If the animal source of manufacturing materials cannot be certified, the material should not be used to manufacture human or animal drugs or biological products. Alternatively, the materials should be tested for the presence of dioxins or PCBs prior to use. One analytical method suitable for foods that may be adapted for analyzing PCBs in pharmaceuticals can be found in the FDA's Pesticide Analytical Manual, Vol. 1, Chap. 3, sect. 303 or 304.2
If products have already been produced using materials that cannot be certified, PCB or dioxin testing of the final product should be performed. If the presence of PCBs or dioxins is detected, manufacturers should contact the appropriate contact person listed below to discuss whether the release of the product is acceptable.
The Agency is conducting a sampling and testing program for dioxins and PCBs in drugs and biologics originating from EU countries.
Contact Persons
For animal drug products, contact John Matheson, Center for Veterinary Medicine, 301-827-6649.
For human drug products, contact Eric Duffy, Center for Drug Evaluation and Research, 301-827-7310.
For biological products, contact Christopher Joneckis, Center for Biologics Evaluation and Research, 301-827-5138.
1 This guidance has been prepared by the Food and Drug Administration.
2 This is available on the FDA Web site.
|
