This guidance document is being distributed for comment purposes only Although you can comment on any guidance at any time, to ensure that the agencies consider your comment on this draft guidance before it begins work on the final version of the guidance, submit written or electronic comments on the draft guidance by April 12, 2009. Submit written comments to the Division of Dockets Management (HFA-305), Food and Drug Administration, U.S. Department of Health and Human Services, 5630 Fishers Lane, Room 1061, Rockville, MD 20852. All comments should be identified with the docket number listed in the notice of availability that is published in the Federal Register. Submit electronic comments to http://www.regulations.gov. For single copies of this draft guidance, please contact: Office of Policy and Planning, Food and Drug Administration, U.S. Department of Health and Human Services 10903 New Hampshire Avenue, White Oak Building 1, Silver Spring, MD 20993, (301) 796-4840. For questions regarding this draft document, contact Jeffrey Shuren, Office of Policy and Planning, Food and Drug Administration, (301) 796-4840. U.S. Department of Health and Human
Services (Food and Drug Administration) January 2009 GOOD IMPORTER PRACTICES This draft guidance document, when finalized, will represent the current thinking of the United States Department of Agriculture, Department of Commerce, Department of Health and Human Services (Food and Drug Administration), Department of Homeland Security, Department of Transportation, Consumer Product Safety Commission, Environmental Protection Agency, and the Office of United States Trade Representative (hereinafter agencies) on this topic. It does not create or confer any rights for or on any person and does not operate to bind the agencies or the public. You may use an alternative approach if the approach satisfies the requirements of the applicable statutes and regulations. If you want to discuss an alternative approach, please contact the appropriate agency staff. IntroductionHelping ensure imported products are in compliance with applicable U.S. statutes and regulations is a shared responsibility between the public and private sectors. To that end, it is important that importers have practices in place that can prevent or detect potential problems at critical points along the product’s life cycle to avoid placing the U.S. consumer at risk. Recognizing this, many importers have already developed practices to prevent or detect and control problems that can occur in foreign-sourced products, ingredients and components (hereinafter products). This guidance document provides general recommendations to importers on possible practices and procedures they may follow to increase the likelihood the products they import are in compliance with applicable U.S. safety and security requirements.1 For example, at various points in a product’s life cycle – growing, harvesting, designing, manufacturing, processing, packing, receiving, storing, transporting, importing, and distributing – it may be appropriate for companies to consider implementing preventive controls to decrease the risk of the product causing harm to people, animals, and/or the environment. The recommendations provided here are intended to promote and facilitate an assessment by importers of the product’s life cycle, so the importer may make sound decisions about how best to address the product’s potential to cause harm and to facilitate compliance with U.S. requirements. Although this guidance relates to requirements and practices pertaining to product safety, importers should also take steps to help ensure that the products they bring into the United States comply with other applicable legal requirements. The recommendations in this guidance do not supersede the federal, state, and/or local statutes or regulations that apply to the product(s) being imported. The recommendations in this guidance may also assist importers in preventing unauthorized access, such as to products, facilities, and records. However, importers may need to take additional security measures. This draft guidance does not address those measures. This draft guidance document would not establish legally enforceable rights or responsibilities. Instead, this guidance document, when finalized, would describe the current thinking of U.S. federal departments and agencies on a topic, and readers should view it only as recommendations, unless the document cites specific regulatory or statutory requirements. The use of the word “should” means that something is suggested or recommended, but not required. Nothing in this document is intended to affect the importer’s responsibility to comply with all applicable requirements found in U.S. statutes and regulations. Interagency Working Group on Import SafetyOn July 18, 2007, President Bush issued Executive Order 13439,2 to establish the Interagency Working Group on Import Safety (Working Group). On September, 10, 2007, the Working Group presented a report to the President entitled Protecting Consumers Every Step of the Way: A Strategic Framework for Continual Improvement in Import Safety (Strategic Framework).3 The Strategic Framework proposed a new approach to ensure the safety of imported products consumed and used by Americans. It noted that "[t]he challenges presented by the increasingly global economy and growing import volumes require a paradigm shift from an intervention, border-focused strategy to a life-cycle approach that stresses a risk-based approach to prevention with verification that identifies high-risk segments of the product life cycle and verifies the safety of products at those important phases. With this shift, the U.S. import process will change from viewing a ‘snapshot’ of the product at the border to achieving a real-time ‘video’ across the product’s life cycle at the most appropriate points of production and distribution." The approach outlined in the Strategic Framework is based on six building blocks,4 and the three organizing principles of prevention of harm, intervention when risks are identified, and response after harm has occurred. The Strategic Framework recognized that "[t]he U.S. government must work with the private sector to adopt an approach to import safety that builds safety into manufacturing and distribution processes. Producers and the importing community will play a key role in accomplishing this objective by implementing preventive approaches and requiring these approaches from their suppliers. In addition, third-party certifications and testing requirements can play an important role in this area, as can credible manufacturer supply-chain management programs." On November 6, 2007, the Working Group released an Action Plan for Import Safety: A Roadmap for Continual Improvement (Action Plan).5 The Action Plan contained 14 broad recommendations and 50 specific short- and long-term action steps to better protect consumers and enhance the safety of the increasing volume of imports entering the United States. The Action Plan stressed the importance of the private sector’s responsibility for the safety of its products and compliance with U.S. standards. It also recognized the importance of private-sector mechanisms and experience and laid a foundation for ongoing, substantive public-private collaboration. The public and private sectors have a shared interest in import safety, and substantive improvement will require the careful collaboration of the entire importing community. Action Step 3.1 of the Action Plan recommended that “[t]he federal government should work with the importing community and other members of the public to develop Good Importer Practices and issue guidance with respect to particular product categories. The focus of these practices will be to ensure that imported products meet U.S. safety standards, as well as to promote effective supply-chain management.” The Action Plan recommended that “[t]hese practices be risk-based and provide concrete guidance to the importing community for evaluating imported products. This evaluation would be based on due diligence and preventive control principles.” The federal government is issuing this guidance in response to the recommendation in Action Step 3.1. It provides principles and recommendations that may apply to imported products generally, and will help ensure that federal agencies and importers adopt a consistent approach. Individual agencies may issue more specific guidance directed at particular product categories to provide more targeted and detailed recommendations. Developing Good Importer Practices can assist the entire importing community in taking appropriate steps to ensure the safety of the products they bring into the United States. ScopeThis Good Importer Practices guidance is intended for use by the importer that initiates or causes the entry or attempted entry of foreign-sourced products into the U.S. or the reimportation of U.S.-made products (American Goods Returned) for commercial purposes or distribution. However, importers who are not bringing in a product for commercial purposes or distribution should have adequate control measures to prevent the distribution of the product into U.S. markets unless the product meets all U.S. requirements. Parties other than importers associated with import transactions might also be subject to U.S. requirements. To promote safety of imported products, these parties (e.g., retailers, manufacturers) should also carefully consider the guidance set forth in this document. Hazards that may place consumers at risk can arise at any point during a product’s life cycle. This guidance document provides recommendations concerning preventive controls firms can implement to mitigate such hazards, and to help ensure imported products are safe and are compliant with U.S. laws and regulations. The recommendations contained in this guidance are designed to anticipate the sources of product hazard that importers may face. We recognize that different goods carry different risks and potential hazards. We encourage importers to tailor these recommendations to their specific situations by adopting the criteria that will most effectively manage the risks that they face and best protect consumers. Further, we recognize that the size and scope of importers’ resources vary enormously. As such, large-scale importers may have greater challenges but also greater resources and influence to minimize risk. While some of the following recommendations may be impractical for some small-scale importers, each importer should take appropriate steps to ensure the safety of its products. In general, we recommend that importers:
Importers should consider instituting practices to identify and minimize risks. Determining the sources of greatest potential risk in a product’s life cycle helps to direct attention to the areas where they can have the greatest positive impact to ensure the safety the product. Importers should put into place controls for known vulnerabilities, such as microbiological contamination and product defects, and monitor for other risks, such as counterfeiting or intentional contamination. Good Importer Practices – Principles and RecommendationsBecause of the wide variety of products and their production processes, the regulatory systems that apply to particular products, and the range of product and importer relationships, it is difficult to develop a set of detailed recommendations that fits every product. However, in developing these recommendations, members of the Working Group did consider the complexity of product life cycles and production processes, as well as the different regulatory frameworks to which various products can be subject. Not all recommendations are appropriate or feasible for every product, and for every importer, but we suggest that importers identify and understand potential risks before deciding to import a particular product. We also recognize that importers could already be using other “best practices” that provide assurance that their products are in compliance with U.S. requirements, and thus are not advising that these importers necessarily modify their practices. However, we believe importers who follow these Good Importer Practices may be less likely to import products that may be harmful to U.S. consumers, and, as a result, may, in some cases, facilitate admissibility determinations, and, therefore, expedite the entry of their products into the United States. However, following these Good Importer Practices does not guarantee compliance with applicable U.S. requirements, or mean that the Government cannot or will not take regulatory or enforcement action regarding compliance with U.S. laws and regulations. These Good Importer Practices are broadly organized under four guiding principles:
Guiding Principle I
|
Product Category |
Relevant Agency |
Applicable Law |
Roles & Responsibilities |
Websites |
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All Products |
Customs and Border Protection (CBP) |
Tariff Act of 1930, Trade Act of 2002, and Security and Accountability for Every (SAFE) Port Act of 2006 |
CBP exercises its regulatory authority to require detailed advance electronic cargo information on arriving goods. Pursuant to its authority to enforce the legal requirements for the entry of merchandise into the U.S. under 19 USC 1484, coupled with its general inspection and examination authorities, e.g., 19 USC 1499, CBP is to sample and hold merchandise on behalf of other government agencies (for example, the Food & Drug Administration and the Consumer Product Safety Commission) that have specific authority to determine the admissibility of these products. CBP exercises enforcement authority using bonding procedures as permitted by the general authority under 19 USC 1623. CBP also has authority under the Tariff Act, particularly 19 USC 1595a(c) to seize merchandise that is imported in violation of any health, safety or conservation prohibition. |
|
Engines and Vehicles (highway and off-road)
Motor Vehicles (on-road) and Motor Vehicle Equipment |
Environmental Protection Agency (EPA) |
Clean Air Act (CAA) |
EPA establishes and enforces regulations that set air pollution emission standards. Vehicles and engines must be certified to meet these standards. Importation of uncertified vehicles or engine-driven equipment without a valid exemption or exclusion is prohibited. |
http://
www.epa.gov/compliance/ |
National Highway Traffic Safety Administration (NHTSA)/U.S. Department of Transportation (DOT) |
National Traffic and Motor Vehicle Safety Act |
NHTSA issues and enforces the Federal motor vehicle safety standards (FMVSS), which establish minimum performance requirements for the safety systems and components on vehicles that are primarily manufactured for use on public roads (motor vehicles) and for certain items of motor vehicle equipment (such as tires, automotive lighting equipment, motorcycle helmets, and child restraints). NHTSA regulates the importation of motor vehicles and regulated items of motor vehicle equipment to ensure compliance with the FMVSS. NHTSA also investigates suspected safety-related defects and noncompliance with the FMVSS. If a motor vehicle or item of motor vehicle equipment contains such a defect or noncompliance, the manufacturer must notify affected owners of the defect or noncompliance and remedy the defect or noncompliance without charge. Manufacturers who fail to furnish notification and remedy may be ordered by NHTSA to do so, and be subject to civil penalties. |
http://www.nhtsa.gov |
|
Fuels and Fuel Additives |
EPA |
CAA |
EPA establishes and enforces regulations requiring that each manufacturer or importer of gasoline, diesel fuel, or a fuel additive for use in motor vehicles, must have its product registered by EPA prior to its introduction into commerce. Registration involves providing a chemical description of the product and certain technical, marketing and health-effects information. This allows EPA to identify the likely combustion and evaporative emissions. EPA also has established and enforces regulations associated with the composition and physical properties of finished gasoline, and onroad and offroad diesel fuel such as sulfur and benzene content. Importers must be registered with EPA and meet these requirements. Importers of renewable fuels must also be registered with EPA and meet specific reporting requirements. |
http://www.epa.gov/compliance/ |
Ozone-Depleting Substances |
EPA |
CAA |
EPA regulates the import of controlled ozone
depleting substances. |
http://www.epa.gov/compliance/ |
Pesticides |
EPA |
Federal Insecticide, Fungicide, and Rodenticide Act (FIFRA) |
FIFRA requires all pesticide products (with limited exceptions) to be registered by the United States, and in compliance with FIFRA including requirements for bearing labels/labeling approved by EPA and product composition requirements. Unregistered products and products determined not to meet EPA requirements may be denied entry. Any product being sold or distributed in the United States must be in compliance with these requirements. If not, they may be subject to penalties, Stop Sale, Use, or Removal Orders, and seizure. |
http://www.epa.gov/compliance/ |
Food |
EPA |
Federal Food, Drug, and Cosmetic Act (FFDCA) |
Under the FFDCA EPA sets “tolerances” (maximum residue limits) for pesticides in both domestic and imported food, to ensure the levels of pesticides in food are safe. U.S. Food and Drug Administration (FDA) and U.S. Department of Agriculture (USDA) are responsible for enforcing EPA established pesticide tolerances on domestic and imported food to ensure any residues detected are within these tolerances. |
http://www.epa.gov/compliance/ |
FDA |
Federal Food, Drug, and Cosmetic Act (FFDCA) Public Health Service Act (PHS Act) Fair Packaging and Labeling Act (FPLA) |
FDA regulates all food products (except meat, poultry, and processed egg products), including dietary supplements. In general, FDA regulates these products using a post-market system to help ensure that food is not adulterated or misbranded. In addition, food and color additives must be approved by FDA before marketing, as must use of health and nutrient content claims. Further, infant formula, food contact substances, and certain new dietary ingredients used in dietary supplements are subject to premarket notification requirements, and low acid canned foods and acidified foods are subject to requirements to file with FDA. |
||
USDA |
Federal Meat Inspection Act (FMIA) Poultry Products Inspection Act (PPIA) Egg Products Inspection Act (EPIA) |
FSIS regulates imported meat, poultry, and
egg products. Imported products are subject to the same food safety
and processing standards applied to U.S. domestic products. These
standards ensure that meat, poultry, and egg products in U.S. commerce
are safe, wholesome, unadulterated, properly labeled, and correctly packaged. |
||
U.S. Department of Commerce (DOC)/National Oceanic and Atmospheric Administration (NOAA) National Marine Fisheries Service (NMFS) |
Agricultural Marketing Act |
The U.S. Department of Commerce (NOAA/NMFS)
provides a voluntary inspection program to the seafood industry to assist
in the assurance of compliance with food regulations. |
||
Chemical Substances |
EPA |
Toxic Substances Control Act (TSCA) |
EPA is responsible for regulating the safety of chemical substances manufactured, imported, processed, distributed, used, and disposed in the United States. EPA (1) reviews new chemicals before manufacture; (2) requires necessary testing of chemicals by manufacturers, importers, and processors where risks or exposures of concern are found; (3) may restrict manufacture, import, processing, use, distribution, or disposal of chemicals to mitigate unreasonable risks; and (4) works to ensure that imported chemicals are in compliance. |
http://www.epa.gov/compliance/ |
Consumer Products |
Consumer Product Safety Commission (CPSC) |
Consumer Product Safety Act (CPSA) |
CPSC has jurisdiction over approximately
15,000 types of consumer products. The CPSA defines consumer product
broadly to include any article or component part thereof, sold to consumers
or for personal use by consumers, in or around a permanent or temporary
household or residence, a school, in recreation, or otherwise. (Generally
excluded from CPSC's jurisdiction are food, drugs, cosmetics, medical
devices, tobacco products, firearms and ammunition, motor vehicles, pesticides,
aircraft, boats and fixed site amusement rides.) Several other
Acts provide authority for CPSC to regulate specific products such as
gasoline cans and pool drain covers under the CPSA. |
|
Hazardous Substance |
CPSC |
Federal Hazardous Substances Act (FHSA) |
The FHSA requires that certain hazardous
household products ("hazardous substances") bear cautionary
labeling to alert consumers to the potential hazards that those products
present and to inform them of the measures they need to protect themselves
from those hazards. Any product that is toxic, corrosive, flammable or
combustible, an irritant, a strong sensitizer, or that generates pressure
through decomposition, heat, or other means requires labeling, if the
product may cause substantial personal injury or substantial illness
during or as a proximate result of any customary or reasonable foreseeable
handling or use, including reasonable foreseeable ingestion by children. |
|
Flammable Fabrics |
CPSC |
Flammable Fabrics Act (FFA) |
The FFA regulates the manufacture of highly flammable clothing, such as brushed rayon sweaters and children's cowboy chaps as well as interior furnishings, paper, plastic, foam and other materials used in wearing apparel and interior furnishings. Under the FFA, CPSC can issue mandatory flammability standards. Standards have been established for the flammability of clothing textiles, vinyl plastic film (used in clothing), carpets and rugs, children's sleepwear and mattresses and mattress pads. It is unlawful to manufacture for sale or import into the United States any product, fabric, or related material that fails to conform to an applicable standard issued under the FFA. The product certification requirements noted above in the discussion of the CPSA also apply to products regulated under the FHSA. |
|
Certain Household Substances |
CPSC |
The Poison Prevention Packaging Act (PPPA) |
The PPPA requires a number of household substances to be packaged in child-resistant packaging. These include certain types of chemical and cosmetic products; mouthwash products and drugs and dietary supplements. The packaging required by the PPPA must be designed or constructed to be significantly difficult for children under five years of age to open within a reasonable time, and not difficult for normal adults to use properly. The CPSC has issued regulations defining which products require child resistant packaging as well as testing protocols to verify the effectiveness of the child-resistant packaging feature. The product certification requirements noted above in the discussion of the CPSA also apply to products required by CPSC regulations to be packaged in child-resistant packaging. |
|
Cosmetics |
FDA |
FFDCA |
FDA regulates cosmetics to help ensure that
they are not adulterated or misbranded. In general, FDA's regulation
of cosmetics is post-market, except that color additives used in cosmetics
require pre-approval. With the exception of a few prohibited or
restricted ingredients, cosmetic manufacturers may use any raw material
as a cosmetic ingredient, as long as the ingredient does not adulterate
the product. |
|
Drugs |
FDA |
FFDCA |
FDA has the responsibility to ensure that human and animal drugs are safe, effective, and properly labeled. All drugs sold in the United States must meet various requirements of the FFDCA, including registration and listing, new drug approval, misbranding, and adulteration provisions, where applicable. FDA performs both pre-market approval inspections and Good Manufacturing Practices (GMPs) inspections to assess compliance with applicable requirements. |
http://www.fda.gov/cder/index.html
|
Medical Devices |
FDA |
FFDCA |
FDA’s regulation of medical devices includes registration of establishments, listing of devices, the requirement that devices be manufactured in accordance with the quality system regulation, reporting of adverse events, and premarket notification (510(k)) or premarket approval (PMA), if applicable. As with drugs, FDA performs both pre-market approval inspections and Quality Systems Regulations (QSRs) inspections to assess compliance. In addition, FDA regulates radiation-emitting electronic products (medical and non-medical) such as lasers, x-ray systems, ultrasound equipment, microwave ovens and color televisions. Regulatory requirements for these products include performance standards, labeling, and submission of radiation safety product reports.
|
http://www.fda.gov/cdrh/index.html
|
Biologics, Blood, and Vaccines |
FDA |
FFDCA PHS Act |
FDA regulates biological products, such as blood and blood products, vaccines, allergenics, and cellular and gene therapies. Such biological products must be approved, which requires that the products are demonstrated to be “safe, pure, and potent” and the facilities involved in production meet applicable standards. In addition, because biological products also meet the definition of “drug” or “device” under the FFDCA, they are also subject to certain FFDCA provisions. Biological product standards regulations include specific standards for blood and blood components and general biological product standards for other products. General standards include requirements for lot release and standards regarding potency, general safety testing, sterility testing, purity testing, as well as standards related to testing for communicable disease agents. FDA’s human tissue regulations address registration of manufacturers, donor eligibility, current good tissue practices, reporting adverse reactions and manufacturing deviations, product labeling, imports, and inspection and enforcement. |
http://www.fda.gov/cber/index.html
|
Animal Feed/Feed Ingredients |
FDA |
FFDCA PHS Act |
FDA regulates animal feeds/food in a manner similar to human foods. Non-medicated animal feeds/food are not subject to premarket approval or licensing. Food and color additives require FDA premarket approval. Facilities that manufacture medicated feed must have a FDA approved medicated feed mill license.
|
http://www.fda.gov/cvm/default.html
|
Plumbing Products |
EPA |
Safe Drinking Water Act (SDWA) |
SDWA prohibits the use of any pipe, plumbing fitting, solder, flux, or plumbing fixture used in plumbing that provides water for human consumption that is not “lead free.” SDWA defines lead free for solders and flux as not more than 0.2 percent lead and for pipes, pipe fittings, and well pumps as not more than 8 percent lead. SDWA also requires EPA to work with third party certifiers to develop a testing protocol for leaching of lead from new plumbing fittings and fixtures. In 1994, EPA identified American National Standards Institute (ANSI)/NSF Standard 61 Section 9. |
http://www.epa.gov/compliance/ |