GMPs 2004 Study: Current Food Good Manufacturing Practices (2023)

August 9, 2004

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Current food good manufacturing practices (GMPs) are published in Title 21 of the Code of Federal Regulations, Part 110 (21 CFR 110). GMPs describe the methods, equipment, facilities, and controls for producing processed food. As the minimum sanitary and processing requirements for producing safe and wholesome food, they are an important part of regulatory control over the safety of the nation's food supply. GMPs also serve as one basis for FDA inspections.

The current GMPs are the result of an extended rulemaking process that spanned decades. The following section (Section 1.1) describes when, why, and how the food GMPs were developed and some of the obstacles that were overcome. Table 1-1 summarizes the major events that led to the development of GMPs as they are today. Section 1.2 provides a detailed discussion of the requirements in each of the five subparts of the GMP regulation, and concludes with a table (Table 1-2) outlining the main requirements.

1.1 The Development of Food GMPs

Food safety has been regulated since the mid-1800s and was mostly the responsibility of local and state regulators. However, the Pure Food and Drugs Act, passed by Congress in 1906, marked the first major federal consumer protection law with respect to food processing. The 1906 law prevented interstate and foreign commerce in misbranded or adulterated foods, drinks, or drugs. The intent of the Act was to prevent poisoning and consumer fraud. As more food products were manufactured in subsequent years, however, poor-quality food products and deceptive packaging continued to be produced due to loopholes in the law. Consumers were often unaware of what they were buying until products were opened. Therefore, in 1933, the FDA decided to overhaul the 1906 Act.

In 1938, after a battle about USDA jurisdictions with respect to the Act's enforcement, the Food Drug, and Cosmetic Act (FDCA) replaced the 1906 Act. The FDCA provided the necessary identity and quality standards to protect consumers from fraud. The FDCA provides the regulatory basis for today's food GMPs. Two sections of the FDCA are directly related to conditions in a facility where food has been manufactured.

  • Section 402 (a)(3) specifies that food has been manufactured under such conditions that it is unfit for consumption.
  • Section 402 (a)(4) considers that food may be adulterated if it is prepared, packed, or held under insanitary conditions whereby it may have become contaminated with filth or rendered injurious to health.

These provisions are unlike other parts of Section 402, in that they relate to the conditions of a facility where food is produced or stored. Thus, instead of having to prove that the food is adulterated, insanitary conditions are considered sufficient to show that the food might have become adulterated.

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Given the FDCA's vagueness in establishing violations and thus, the difficulty of enforcing it, FDA began working on draft GMP regulations by the mid-1960s (although others had made the suggestion to do so as early as 1948). The objective of the GMP regulations was to describe general rules for maintaining sanitary conditions that must be followed by all food processing facilities to ensure that the statutory requirements of Section 402(a)(3) and (4) were met. After much industry involvement, including much debate about FDA's authority to adopt rules to carry out the provisions of the FDCA, the GMP regulations for food processing facilities were finally proposed in 1968 (see Table 1-1).

Three broad categories of interrelated issues arose during the development of the GMPs (Dunkelberger, 1995):

  • Concern that the regulations were unduly stringent and especially burdensome for small food companies without necessarily improving the quality or safety of foods.
  • Contention that the GMP regulations must prescribe conditions that "reasonably" relate to insanitary conditions that may contaminate food and render it injurious to health.
  • Assertions that the regulations did not have the force of law.

These first two issues were resolved mostly through the use of more general terms, such as "adequate," "sufficient," and "suitable," rather than hard-line standards. FDA also used "shall" when the agency felt compliance was necessary and "should" when practices in the rule were less obviously related to the statutory requirements of the Act. The third issue became inconsequential when it was proved that FDA did have the statutory authority to promulgate the GMP regulations. The GMP regulations were finalized in April of 1969 and published as Part 128 of the Code of Federal Regulations (CFR). In 1977, Part 128 was recodified and published as Part 110 of the CFR.

The final GMP regulations were very broad, not specifying what exactly a facility must do to comply. This naturally created enforcement problems for the FDA. To address the ambiguity created by the umbrella GMPs, FDA next tried to develop industry-specific GMPs through the mid-1970s. By the late 1970s, however, FDA decided to improve the umbrella GMPs rather than adopting industry-specific GMPs. The revisions were finalized in 1986 and printed in 21 CFR 110. Specific GMPs were also included and printed in 21 CFR Parts 100 through 169 for:

  • Quality control procedures for nutrient content of infant formula (21 CFR 106).
  • Thermally processed low-acid canned foods in hermetically sealed containers (21 CFR 113).
  • Acidified foods (21 CFR 114).
  • Bottled drinking water (21 CFR 129).

In July of 2002, FDA formed a Food GMP Modernization Working Group to examine the effectiveness of current food GMPs given the many changes that have occurred in the food industry since 1986. The Working Group has been researching the impact of food GMPs on food safety, as well as on the impact (including economic consequences) of revised regulations. Part of the group's current effort, as of June 2004, is to find out which elements of the food GMPs are critical to retain and which should be improved. FDA is now holding public meetings to obtain the public comments to assist in this effort.

Table 1-1: Food GMP Development Timeline
1906The Bureau of Chemistry passes the 1906 Pure Food and Drugs Act, prohibiting interstate commerce in misbranded and adulterated foods, drinks, and drugs
1933FDA recommends revising the 1906 Pure Food and Drugs Act
1938FDA passes the 1938 Federal Food, Drugs, and Cosmetics Act, which provides identity and quality standards for food
Mid 1960sFDA decides to clarify the FDCA through GMP regulations
1968FDA proposes food GMP regulations
1969FDA finalizes food GMP regulations
Early 1970sFDA considers promulgating industry-specific regulations
Late-1970sFDA decides to revise the general GMPs rather than adopting industry-specific GMPs
1986FDA publishes revised food GMPs
2002FDA forms Food GMP Modernization Working Group
2004FDA announces effort to modernize food GMPs
Source: Dunkelberger, 1995; FDA, 1981b.

1.2 Key Provisions of Food GMPs

The current GMPs consist of seven subparts, two of which are reserved. The requirements are purposely general to allow individual variation by manufacturers to implement the requirements in a manner that best suit their needs. Table 1-2 summarizes the five written subparts, which are discussed in further detail below.

1.2.1 General Provisions (Subpart A)

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The general provisions in Subpart A of the food GMPs are divided into four sections. The first section defines much of the terminology used in describing GMPs. The terms "shall" and "should" are also defined to differentiate between when compliance is necessary ("shall") and when procedures and practices are not directly related to insanitary conditions as specified in Section 402(4)(a) ("should").

The section on personnel delineates plant and employee responsibilities with regard to personal hygiene. For example, personnel with diseases or other conditions that could contaminate food are to be excluded from manufacturing operations. The section also outlines expectations with respect to personal hygiene and cleanliness, clothing, removal of jewelry and other unsecured objects, glove maintenance, use of hair restraints, appropriate storage of personal items, and restrictions on various activities, such as eating and smoking. The section discusses the need for appropriate food safety education and training in very general terms. The subpart further mandates the assignment of supervisory personnel to ensure compliance.

Currently, establishments that only harvest, store, or distribute raw agricultural commodities are exempt from the requirements of Subpart A, although FDA reserves the right to issue special regulations to address this sector.

1.2.2 Buildings and Facilities (Subpart B)

Subpart B of the food GMPs outlines requirements for the maintenance, layout, and operations of food processing facilities.

Section 110.20 outlines the requirements for adequate maintenance of the grounds, including litter control, waste removal and treatment, and grounds maintenance and drainage. The subpart requires that plants be designed and built to reduce the potential for contamination. Some detail is provided on how to achieve this, but the requirements are largely focused on the end result of a sanitary facility rather than specific practices. The language also includes many general terms to allow flexible implementation of the requirements.

Section 110.35 describes sanitary operations. Physical facilities, equipment, and utensils are to be sanitized in a way that protects against food contamination. Storage of cleaning materials and toxic materials permitted are outlined to prevent contamination with chemicals. The section also briefly addresses pest control and cleaning of various food contact surfaces, as well as the frequency of cleaning.

Section 110.37 describes the requirements for adequate sanitary facilities and controls, including the water supply, plumbing, toilet and hand-washing facilities, and rubbish and offal disposal.

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Some of the requirements of the section are fairly specific, such as the requirement of self-closing doors for toilet facilities, whereas others remain general, such as plumbing of adequate size and design.

1.2.3 Equipment (Subpart C)

Subpart C describes the requirements and expectations for the design, construction, and maintenance of equipment and utensils so as to ensure sanitary conditions. It also adds a specific requirement; an automatic control for regulating temperature or an alarm system to alert employees to a significant change in temperature. Other requirements of the subpart are fairly general and intended to prevent contamination from any source.

1.2.4 Production and Process Controls (Subpart E)

The first section of Subpart E lists the general sanitation processes and controls necessary to ensure that food is suitable for human consumption. It uses more general words (e.g., "adequate," "reasonable," etc.) and covers many aspects not discussed in previous subparts. This section also addresses the monitoring of physical factors (critical control points), such as time, temperature, humidity, pH, flow rate, and acidification.

The second section outlines very general requirements for warehousing and distribution. The section requires finished foods to be stored and distributed under conditions that protect against physical, chemical, and microbial contamination. The container and the food must also be protected from deterioration.

1.2.5 Defect Action Levels (DALs) (Subpart G)

The last subpart of the food GMPs allows FDA to define maximum defect action levels (DALs) for a defect that is natural or unavoidable even when foods are produced under GMPs as set out in the other subparts of the regulations. Generally, these defects are not hazardous to health at low levels; they include rodent filth, insects, or mold. The DALs are defined for individual commodities and may be obtained by request from FDA, which produces a Handbook on Defect Action Levels for Food. They are also available from the FDA Web site Defect Action Levels handbook. Table 1-3 provides examples of the maximum DALs for select food products. Manufacturers are expected to use quality control operations that reduce the level of the defect to the lowest possible levels. Those exceeding maximum DALs will be considered in violation of Section 402 (3)(a) of the FDCA.

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The section bans blending of food with a defect level above a maximum DAL with other food. It also stresses that compliance with DALs does not excuse violations of Section 402(4)(a) of the FDCA or that of the other subparts of 21 CFR 110.

Table 1-2: Summary of 21 CFR Part 110: Current Good Manufacturing Practice in Manufacturing, Packing, or Holding Human Food
Subpart A. General ProvisionsSection 110.3DefinitionsDefinitions of:
  • Acid foods/acidified foods
  • Adequate
  • Batter
  • Blanching
  • Critical control point
  • Food
  • Food-contact surfaces
  • Lot
  • Microorganisms
  • Pest
  • Plant
  • Quality control operation
  • Rework
  • Safe-moisture level
  • Sanitize
  • Shall
  • Should
  • Water activity
Section 110.5Current good manufacturing practice
  • Criteria for determining adulteration
  • Food covered by specific GMPs is also covered by umbrella GMPs
Section 110.10PersonnelRequirements for:
  • Disease control
  • Cleanliness
  • Education and training
  • Supervision of personnel with regards to these requirements
Section 110.19Exclusions
  • Excluded operations (raw agricultural commodities)
  • FDA can issue special regulations to cover excluded operations
Subpart B. Buildings and FacilitiesSection 110.20Plant and Grounds
  • Description of adequate maintenance of grounds
  • Plant construction and design to facilitate sanitary operations and maintenance
Section 110.35Sanitary OperationsRequirements for:
  • Cleaning/sanitizing of physical facilities, utensils, and equipment
  • Storage of cleaning and sanitizing substances
  • Pest control
  • Sanitation of food contact surfaces
  • Storage and handling of cleaned portable equipment and utensils
Section 110.20Sanitary Facilities and ControlsRequirements for:
  • Water supply
  • Plumbing
  • Sewage disposal
  • Toilet facilities
  • Hand-washing facilities
  • Rubbish and offal disposal
Subpart C. EquipmentSection 110.40Equipment and Utensils
  • Requirements for the design, construction, and maintenance of equipment and utensils
Subpart E. Production and Process ControlsSection 110.80Processes and controlsDelineates processes and controls for:
  • Raw materials and other ingredients
  • Manufacturing operations
Section 110.93Warehousing and distributionStorage and transportation of food must protect against contamination and deterioration of the food and its container
Subpart G. Defect Action LevelsSection 110.10
  • FDA has established maximum defect action levels (DALs) for some natural or unavoidable defects
  • Compliance with DALs does not excuse violation of 402 (a)(4)
  • Food containing defects above DALs may not be mixed with other foods
Source: Federal Register 51, 1986.
Table 1-3: Maximum Defect Action Levels for Selected Food Products
Food ProductMaximum Defect Action Level
Allspice (ground)
  • Average of 30 or more insect fragments per 10 grams
  • Average of 1 or more rodent hairs per 10 grams
Broccoli (frozen)
  • Average of 60 or more aphids, thrips, and/or mites per 100 grams
Cocoa beans
  • More than 4% of beans by count are moldy
  • More than 4% of beans by count are insect-infested or insect-damaged
  • More than 6% of beans by count are insect-infested or moldy (NOTE: Level differs when both filth and mold are present)
  • Average of 10 mg or more mammalian excreta per pound
Pitted olives
  • Average of 1.3 percent or more by count of olives with whole pits and/or pit fragments 2 mm or longer measured in the longest dimension
Pineapple juice
  • Average mold count of 15% or more
  • Mold count of any 1 subsample is 40% or more
Tomatoes (canned)
  • Average of 10 or more fly eggs per 500 grams
  • 5 or more fly eggs and 1 or more maggots per 500 grams
  • 2 or more maggots per 500 grams
Source: FDA, 2004.


Dunkelberger, Edward. 1995. The statutory basis for the FDA's food safety assurance programs: From GMP, to emergency permit control, to HACCP. Food and Drug Law Journal 50. 357-383.

Federal Register 51. 1986. Part 110--Current Good Manufacturing Practice in Manufacturing, Packing, or Holding Human Food. Federal Register 51. June 19.

Food and Drug Administration (FDA). 1981a. The Story of the Laws Behind the Labels Part I: 1906 Food and Drugs Act . FDA Consumer. June.

Food and Drug Administration (FDA). 1981b. The Story of the Laws Behind the Labels Part II: 1938 Federal Food, Drugs, and Cosmetics Act. FDA Consumer. June.

Food and Drug Administration (FDA). 1999. Milestones in U.S. Food and Drug Law History. FDA Backgrounder. May 3.

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FDA. 2004. The Food Defect Action Levels. Center for Food Safety and Applied Nutrition. Revised May 1998.

Gould, Wilbur A. 1994. CGMPS/Food Plant Sanitation. CTI Publications, Inc: Baltimore, MD.

Junod, Suzanne White. 1999. The Rise and Fall of Federal Food Standards in the United States: the Case of the Peanut Butter and Jelly Sandwich. Society for the Social History of Medicine. Spring Conference. April 9.


What are current GMPs? ›

What are CGMPs? CGMP refers to the Current Good Manufacturing Practice regulations enforced by the FDA. CGMPs provide for systems that assure proper design, monitoring, and control of manufacturing processes and facilities.

How do GMPs contribute to food safety? ›

Good Manufacturing Practices* (GMPs) are the basic operational and environmental conditions required to produce safe foods. They ensure that ingredients, products and packaging materials are handled safely and that food products are processed in a suitable environment.

What are the 5 main components of good manufacturing practice? ›

5 Key Components of Good Manufacturing Practices
  • Primary Materials and Products.
  • Premises.
  • People.
  • Procedures.
  • Processes.
6 Jul 2021

What topics does GMPs cover? ›

GMP covers all aspects of production from the starting materials, premises, and equipment to the training and personal hygiene of staff. Detailed written procedures are essential for each process that could affect the quality of the finished product.

Does FDA issue GMP certificates? ›

The FDA regularly audits pharmaceutical manufacturers to ensure that they are cGMP compliant. However, the FDA does not certify manufacturers, they only determine if the business is in compliance or not. A manufacturer must demonstrate that they are following the thorough standards set by cGMP in order to be certified.

What are the 10 Principles of GMP in food industry? ›

What Are the 10 Principles of GMP?
  • Write detailed, step-by-step procedures. ...
  • Follow established procedures. ...
  • Document everything. ...
  • Validate the SOPs and specs. ...
  • Integrate quality and safety into equipment and facilities. ...
  • Maintain equipment and facilities. ...
  • Establish, develop, and demonstrate job competence. ...
  • Ensure cleanliness.
2 Sept 2021

What are GMPs for food manufacturing? ›

What is GMP? GMP, an acronym that stands for Good Manufacturing Practices, establishes the operational conditions and requirements necessary to ensure hygiene throughout the food chain and for the production thereof.

Why are GMPs so important? ›

Good Manufacturing Practices are a critical system that all manufacturing facilities should implement. They help ensure the proper design, monitoring, and control of the manufacturing processes and facilities. Companies that adhere to these standards help to assure the identity, strength, and quality of their products.

Why is GMP needed in food industry? ›

GMP requires a quality approach to manufacturing, enabling companies to minimize or eliminate instances of contamination, mixups, and errors. This in turn, protects the consumer from purchasing unsafe and poor quality products.

How many types of GMP are there? ›

Assuring quality of a manufactured product requires certain procedures and standards. In many industries, these procedures and standards are often referred to as Good Manufacturing Practices, or GMPs.

What is 5S in food industry? ›

Sort, straighten, shine, standardize, and sustain.

5S principles are based on the idea that a well organized and clean workplace increases employee satisfaction, promotes worker safety, and decreases product waste.

What are the 10 Principles of GMP? ›

Principles of GMP
  • 10 Principle of Good Manufacturing Practises. ...
  • PRINCIPLE 1: Step by step written procedures. ...
  • PRINCIPLE 2: Follow procedures. ...
  • PRINCIPLE 3 Document work. ...
  • PRINCIPLE 4 Validate work. ...
  • PRINCIPLE 5 Integrate productivity, quality & safety into facilities & equipment. ...
  • PRINCIPLE 6 Maintain facilities & equipment.
1 Jun 2019

What is GMP audit checklist? ›

A Good Manufacturing Practices (GMP) audit checklist is a tool used by manufacturers to ensure that food, pharmaceutical, medical, and cosmetic products are of consistent quality and in compliance with manufacturing standards.

WHO GMP guidelines list? ›

General guidelines of WHO useful for pharmaceutical manufacturing.
These guidelines cover all the pharmaceutical topics as:
  • Process validation.
  • Cleaning validation.
  • Analytical method validation.
  • DQ, IQ, OQ, PQ of equipment.
  • Water system validation.
  • HVAC validation.
  • Computer system validation.
  • Market complaint handling.

Why do we need GMPS? ›

GMP prevents errors that cannot be eliminated through quality control of the finished product. Without GMP it is impossible to be sure that every unit of a medicine is of the same quality as the units of medicine tested in the laboratory.


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