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Good manufacturing practice

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Current good manufacturing practices (cGMP) are those conforming to the guidelines recommended by relevant agencies. Those agencies control the authorization and licensing of the manufacture and sale of food and beverages,[1] cosmetics,[2] pharmaceutical products,[3] dietary supplements,[4] and medical devices.[5] These guidelines provide minimum requirements that a manufacturer must meet to assure that their products are consistently high in quality, from batch to batch, for their intended use.

Good Manufacturing Practice emerged in response to serious incidents of harm caused by contaminated, adulterated, or improperly manufactured products. Major incidents include: deaths from Elixir Sulfanilamide in 1937, thalidomide-induced birthdefects 1957-1961, poliomyelitis infections from improperly prepared vaccines in 1955, and Dalkon Shield-induced septicemia in the 1970's.

These incidents resulted in hundreds of deaths, infections, and birth defects. Complete timelines show the emergence of Good Manufacturing Practices alongside these incidents, starting from 1938 in the US and 1970s internationally.[6]

The rules that govern each industry may differ significantly; however, the main purpose of GMP is always to prevent harm from occurring to the end user.[2] Additional tenets include ensuring the end product is free from contamination, that it is consistent in its manufacture, that its manufacture has been well documented, that personnel are well trained, and that the product has been checked for quality more than just at the end phase.[2] GMP is typically ensured through the effective use of a quality management system (QMS).[1]: "The Basis for GMP",  [2]

Good manufacturing practice, along with good agricultural practice, good laboratory practice and good clinical practice, are overseen by regulatory agencies in the United Kingdom, United States, Canada, various European countries, China, India and other countries.

High-level details

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Good manufacturing practice guidelines provide guidance for manufacturing, testing, and quality assurance in order to ensure that a manufactured product is safe for human consumption or use. Many countries have legislated that manufacturers follow GMP procedures and create their own GMP guidelines that correspond with their legislation.

All guidelines follow a few basic principles:[2][7]

  • Manufacturing facilities must maintain a clean and hygienic manufacturing area.
  • Manufacturing facilities must maintain controlled environmental conditions in order to prevent cross-contamination from adulterants and allergens that may render the product unsafe for human consumption or use.
  • Manufacturing processes must be clearly defined and controlled. All critical processes are validated[8] to ensure consistency and compliance with specifications.
  • Manufacturing processes must be controlled, and any changes to the process must be evaluated. Changes that affect the quality of the drug are validated[9] as necessary.
  • Instructions and procedures must be written in clear and unambiguous language using good documentation practices.
  • Operators must be trained to carry out and document procedures.
  • Records must be made, manually or electronically, during manufacture that demonstrate that all the steps required by the defined procedures and instructions were in fact taken and that the quantity and quality of the food or drug was as expected. Deviations must be investigated and documented.
  • Records of manufacture (including distribution) that enable the complete history of a batch to be traced must be retained in a comprehensible and accessible form.
  • Any distribution of products must minimize any risk to their quality.
  • A system must be in place for recalling any batch from sale or supply.
  • Complaints about marketed products must be examined, the causes of quality defects must be investigated, and appropriate measures must be taken with respect to the defective products and to prevent recurrence.

Good manufacturing practice is recommended with the goal of safeguarding the health of consumers and patients as well as producing quality products. In the United States, a food or drug may be deemed "adulterated" if it has passed all of the specifications tests but is found to be manufactured in a facility or condition which violates or does not comply with current good manufacturing guideline.

GMP standards are not prescriptive instructions on how to manufacture products. They are a series of performance based requirements that must be met during manufacturing.[10] When a company is setting up its quality program and manufacturing process, there may be many ways it can fulfill GMP requirements. It is the company's responsibility to determine the most effective and efficient quality process that both meets business and regulatory needs.[1]: "Decision Makers' Summary",  [2]

Regulatory agencies have recently begun to look at more fundamental quality metrics of manufacturers than just compliance with basic GMP regulations. US-FDA has found that manufacturers who have implemented quality metrics programs[11] gain a deeper insight into employee behaviors that impact product quality.

In its Guidance for Industry "Data Integrity and Compliance With Drug CGMP" US-FDA states “it is the role of management with executive responsibility to create a quality culture where employees understand that [[data integrity[12]]] is an organizational core value and employees are encouraged to identify and promptly report data integrity issues.”[13] Australia's Therapeutic Goods Administration has said that recent data integrity failures have raised questions about the role of quality culture in driving behaviors.[14] In addition, non-governmental organizations such as the International Society for Pharmaceutical Engineering (ISPE) and the Parenteral Drug Association (PDA) have developed information and resources to help pharmaceutical companies better understand why quality culture is important and how to assess the current situation within a site or organization.[15]

Guideline versions

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GMP is enforced in the United States by the U.S. Food and Drug Administration (FDA), under Title 21 CFR. The regulations use the phrase "current good manufacturing practices" (CGMP) to describe these guidelines.[16][17][18][19] Courts may theoretically hold that a product is adulterated even if there is no specific regulatory requirement that was violated as long as the process was not performed according to industry standards.[20] However, since June 2007, a different set of CGMP requirements have applied to all manufacturers of dietary supplements, with additional supporting guidance issued in 2010.[4] Additionally, in the U.S., medical device manufacturers must follow what are called "quality system regulations" which are deliberately harmonized with ISO requirements, not necessarily CGMPs.[18]

The World Health Organization (WHO) version of GMP is used by pharmaceutical regulators and the pharmaceutical industry in over 100 countries worldwide, primarily in the developing world.[3] The European Union's GMP (EU GMP) enforces similar requirements to WHO GMP, as does the FDA's version in the US. Similar GMPs are used in other countries, with Australia, Canada, Japan, Saudi Arabia, Singapore, Philippines], Vietnam and others having highly developed/sophisticated GMP requirements.[21] In the United Kingdom, the Medicines Act (1968) covers most aspects of GMP in what is commonly referred to as "The Orange Guide," which is named so because of the color of its cover; it is officially known as Rules and Guidance for Pharmaceutical Manufacturers and Distributors.[22]

Since the 1999 publication of Good Manufacturing Practice for Active Pharmaceutical Ingredients, by the International Conference on Harmonization (ICH), GMPs now apply in those countries and trade groupings that are signatories to ICH (the EU, Japan and the U.S.), and applies in other countries (e.g., Australia, Canada, Singapore) which adopt ICH guidelines for the manufacture and testing of active raw materials.[21]

Enforcement

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Within the European Union GMP inspections are performed by National Regulatory Agencies. GMP inspections are performed in Canada by the Health Products and Food Branch Inspectorate;[23] in the United Kingdom by the Medicines and Healthcare products Regulatory Agency (MHRA);[24] in the Republic of Korea (South Korea) by the Ministry of Food and Drug Safety (MFDS);[25] in Australia by the Therapeutic Goods Administration (TGA);[26] in Bangladesh by the Directorate General of Drug Administration (DGDA);[27] in South Africa by the Medicines Control Council (MCC);[28] in Brazil by the National Health Surveillance Agency (ANVISA);[29] in India by state Food and Drugs Administrations (FDA), reporting to the Central Drugs Standard Control Organization;[30] in Pakistan by the Drug Regulatory Authority of Pakistan;[31] in Nigeria by NAFDAC;[32] and by similar national organizations worldwide. Each of the inspectorates carries out routine GMP inspections to ensure that drug products are produced safely and correctly. Additionally, many countries perform pre-approval inspections (PAI) for GMP compliance prior to the approval of a new drug for marketing.

CGMP inspections

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Regulatory agencies (including the FDA in the U.S. and regulatory agencies in many European nations) are authorized to conduct unannounced inspections, though some are scheduled.[16][22][25][26][27][28][30][31][32] FDA routine domestic inspections are usually unannounced, but must be conducted according to 704(a) of the Food, Drug and Cosmetic Act (21 USCS § 374), which requires that they are performed at a "reasonable time". Courts have held that any time the firm is open for business is a reasonable time for an inspection.[33]

Other good practices

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Other good-practice systems, along the same lines as GMP, exist:

Collectively, these and other good-practice requirements are referred to as "GxP" requirements, all of which follow similar philosophies. Other examples include good guidance practice and good tissue practice.

See also

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References

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  1. ^ a b c Institute of Food Science & Technology (2013). Food and Drink - Good Manufacturing Practice - A Guide to its responsible management. London: Wiley-Blackwell. ISBN 9781118318232 – via Google Books (Preview).
  2. ^ a b c d e f Moore, Iain (2009). "Chapter 5: Manufacturing Cosmetic Ingredients According to Good Manufacturing Principles". In Lintner, Karl (ed.). Global Regulatory Issues for the Cosmetic Industry. Vol. 2. Norwich, New York: William Andrew. pp. 79–92. ISBN 9780815519645 – via Google Books (Preview).
  3. ^ a b Nally, J.D., ed. (2007). Good Manufacturing Practices for Pharmaceuticals (6th ed.). CRC Press. p. 424. ISBN 9781420020939.
  4. ^ a b "Guidance for Industry: Current Good Manufacturing Practice in Manufacturing, Packaging, Labeling, or Holding Operations for Dietary Supplements; Small Entity Compliance Guide". U.S. Food and Drug and Administration. 12 November 2017. Retrieved 2 February 2018.
  5. ^ Ramakrishna, S.; Tian, L.; Wang, C.; et al., eds. (2015). "Chapter 3.: Quality management systems for medical device manufacture". Medical Devices: Regulations, Standards and Practices. Woodhead Publishing Series in Biomaterials. Vol. 103. Elsevier. pp. 49–64. ISBN 9780081002919.
  6. ^ "Why does Good Manufacturing Practice exist?". SystemValidation. Retrieved 29 September 2024.
  7. ^ World Health Organization (2007). "Chapter 1: WHO good manufacturing practices: Main principles for pharmaceutical products". Quality Assurance of Pharmaceuticals: A compendium of guidelines and related materials - Good manufacturing practices and inspection. Vol. 2 (2nd updated ed.). WHO Press. pp. 17–18. ISBN 9789241547086.
  8. ^ "What is Validation?". SystemValidation. Retrieved 29 September 2024.
  9. ^ "What is Validation?". SystemValidation. Retrieved 29 September 2024.
  10. ^ "Performance-Based Safety Regulation | Policy Studies". www.trb.org. Retrieved 2020-12-28.
  11. ^ Center for Drug Evaluation and Research (2019-12-20). "Frequently Asked Questions regarding the Quality Metrics Site Visit and Feedback Programs". FDA.
  12. ^ "Data Integrity & Audit Trails". SystemValidation. Retrieved 29 September 2024.
  13. ^ US Food and Drug Administration (2018). "Data Integrity and Compliance With Drug CGMP Questions and Answers Guidance for Industry". US-Food and Drug Administration. Retrieved October 9, 2021.
  14. ^ Australian Government Department of Health Therapeutic Goods Administration (2018-08-09). "Presentation: Driving a GMP / Quality Culture to provide supporting evidence of better business outcomes". Therapeutic Goods Administration (TGA). Retrieved 2020-12-10.[permanent dead link‍]
  15. ^ Frederick, Tami (2019). "ISPE – PDA Guide to Improving Quality Culture in Pharmaceutical Manufacturing Facilities" (PDF). International Society for Pharmaceutical Engineering. Retrieved 2020-12-09.
  16. ^ a b "Facts About the Current Good Manufacturing Practices (CGMPs)". U.S. Food and Drug Administration. 6 October 2017. Retrieved 2 February 2018.
  17. ^ "Current Good Manufacturing Practices (CGMPs)". U.S. Food and Drug Administration. 27 December 2017. Retrieved 2 February 2018.
  18. ^ a b "Quality System (QS) Regulation/Medical Device Good Manufacturing Practices". U.S. Food and Drug Administration. 2 February 2018. Retrieved 2 February 2018.
  19. ^ "Draft Guidance for Industry: Cosmetic Good Manufacturing Practices". U.S. Food and Drug Administration. 3 November 2017. Retrieved 2 February 2018.
  20. ^ "US CFR Title 21 §210.1(b) Status of current good manufacturing practice regulations". Electronic Code of Federal Regulations. Retrieved 24 August 2017.
  21. ^ a b Cartwright, A.C.; Matthews, B.R., eds. (2010). "Preface". International Pharmaceutical Product Registration (2nd ed.). CRC Press. pp. vi–x. ISBN 9781420081831.
  22. ^ a b Medicines and Healthcare products Regulatory Agency. "Rules and Guidance for Pharmaceutical Manufacturers and Distributors 2017". Pharmaceutical Press. Retrieved 2 February 2018.
  23. ^ "Good Manufacturing Practices". Health Canada. Government of Canada. 27 February 2015. Retrieved 2 February 2018.
  24. ^ Medicines and Healthcare products Regulatory Agency (20 October 2017). "Good manufacturing practice and good distribution practice". Gov.uk. Retrieved 2 February 2018.
  25. ^ a b Ministry of Food and Drug Safety (April 2017). "Guide to Drug Approval System in Korea" (PDF). National Institute of Food and Drug Safety Evaluation. Retrieved 2 February 2018.
  26. ^ a b "Good manufacturing practice - an overview". Department of Health, Therapeutic Goods Administration. 29 September 2017. Retrieved 2 February 2018.
  27. ^ a b Anisfeld, M.H.; Kim, E.M.; Aimiuwu, J.; Thumm, M. (May 2015). "Assessment of the Good Manufacturing Practices Inspection Program of the Bangladesh Directorate General of Drug Administration". World Health Organization. Archived from the original on April 29, 2017. Retrieved 2 February 2018.
  28. ^ a b "Guide to Good Manufacturing Practice for Medicines in South Africa" (PDF). Medicines Control Council. August 2010. Retrieved 2 February 2018.
  29. ^ "Draft Technical Resolution nº 42, May 13th 2015" (PDF). World Trade Organization. 13 May 2015. Retrieved 2 February 2018.
  30. ^ a b "Updated list of WHO GMP Certified Manufacturing Units for Certificate of Pharmaceutical Products (COPP) in various States of India as on December 2016". Central Drugs Standard Control Organization. 10 June 2017. Archived from the original on 3 February 2018. Retrieved 2 February 2018.
  31. ^ a b "S.R.O. 1012(I)/2017" (PDF). The Gazette of Pakistan. Government of Pakistan. 9 October 2017. Archived from the original (PDF) on 2 February 2018. Retrieved 2 February 2018.
  32. ^ a b "GMP Guidelines". National Agency for Food and Drug Administration and Control. Archived from the original on 3 February 2018. Retrieved 2 February 2018.
  33. ^ "Guidance for Industry Circumstances that Constitute Delaying, Denying, Limiting, or Refusing a Drug Inspection" (PDF). U.S. Food and Drug Administration. October 2014. Retrieved 2 February 2018.
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