Good laboratory practice (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "Good laboratory practice" in English language version.

refsWebsite

Global rank English rank

23fda.gov

447^th place

338^th place

18web.archive.org

1^st place

8oecd.org

960^th place

854^th place

7europa.eu

68^th place

117^th place

6hma.eu

low place

5doi.org

2^nd place

3ecfr.gov

5,608^th place

3,261^st place

2govinfo.gov

1,998^th place

1,116^th place

2epa.gov

882^nd place

600^th place

1worldcat.org

5^th place

1biopharminternational.com

low place

1planetwaves.net

low place

1who.int

195^th place

302^nd place

1nih.gov

4^th place

1federalregister.gov

2,474^th place

1,469^th place

1regulations.gov

low place

biopharminternational.com

Kevin Robinson for BioPharm International, 1 Aug 2003. GLPs and the Importance of Standard Operating Procedures Archived 21 March 2005 at the Wayback Machine

doi.org

"EU Legislation with Good Laboratory Practice (GLP) Provisions". EU Environmental Legislation: 89–90. March 2024. doi:10.4337/9781781954775.00012. Retrieved June 18, 2024.
Baldeshwiler, Anne (29 July 2003). "History of FDA good laboratory practices". The Quality Assurance Journal. 7 (3): 157–161. doi:10.1002/qaj.228. eISSN 1099-1786. ISSN 1087-8378 – via Wiley Online Library.
"Specific regulatory choices". EU Environmental Legislation: 89–90. doi:10.4337/9781781954775.00012.

dx.doi.org

"EU Legislation with Good Laboratory Practice (GLP) Provisions". EU Environmental Legislation: 89–90. March 2024. doi:10.4337/9781781954775.00012. Retrieved June 18, 2024.
"Specific regulatory choices". EU Environmental Legislation: 89–90. doi:10.4337/9781781954775.00012.

ecfr.gov

"21 CFR Part 58 -- Good Laboratory Practice for Nonclinical Laboratory Studies". www.ecfr.gov. Retrieved 2025-05-15.
"40 CFR Part 160 -- Good Laboratory Practice Standards". www.ecfr.gov. Retrieved 2025-05-15.
"40 CFR Part 792 -- Good Laboratory Practice Standards". www.ecfr.gov. Retrieved 2025-05-15.

epa.gov

US EPA, OECA (2013-07-30). "Good Laboratory Practices Standards Compliance Monitoring Program". www.epa.gov. Retrieved 2024-04-17.
US EPA, OECA (July 30, 2013). "Good Laboratory Practices Standards Compliance Monitoring Program". www.epa.gov.

europa.eu

data.europa.eu

eur-lex.europa.eu

ema.europa.eu

"Good laboratory practice compliance | European Medicines Agency". www.ema.europa.eu. 31 December 2009. Retrieved 2024-06-18.

single-market-economy.ec.europa.eu

"Good Laboratory Practice - European Commission". single-market-economy.ec.europa.eu. Retrieved 2024-06-18.

ec.europa.eu

"DocsRoom - European Commission". ec.europa.eu.

fda.gov

"Good Laboratory Practice (GLP), Proposed Rule, 11/19/1976". U.S. Food and Drug Administration. December 22, 2020 [November 19, 1976]. Archived from the original on December 13, 2019. Retrieved April 23, 2024.
"Good Laboratory Practice (GLP) Final Rule, 12/22/1978". U.S. Food and Drug Administration. December 22, 2020 [December 22, 1978]. Retrieved April 23, 2024.
"Good Laboratory Practice Regulations Management Briefings Post Conference Report". U.S. Food and Drug Administration. February 24, 2020 [August 1979]. Archived from the original on September 30, 2020. Retrieved April 23, 2024.
"Good Laboratory Practice (GLP), Proposed Rule, 10/29/1984". U.S. Food and Drug Administration. December 22, 2020 [October 29, 1984]. Retrieved April 23, 2024.
"Good Laboratory Practice (GLP), Amendment, Final Rule, 9/4/1987". U.S. Food and Drug Administration. December 22, 2020 [September 4, 1987]. Archived from the original on December 13, 2019. Retrieved April 23, 2024.
Commissioner, Office of the (2025-03-25). "Federal Food, Drug, and Cosmetic Act (FD&C Act)". FDA. Archived from the original on May 2, 2019. Retrieved 2025-05-15.
"Bioresearch Monitoring Program (BIMO) Compliance Program 7348.808 Good Laboratory Practice (Nonclinical Laboratories)". U.S. Food and Drug Administration. May 1, 2018. Retrieved April 23, 2024.^{[dead link]}
"Bioresearch Monitoring Program (BIMO) Compliance Program 7348.810 Sponsors and Contract Research Organizations". U.S. Food and Drug Administration. September 15, 2021. Archived from the original on December 14, 2019. Retrieved April 23, 2024.
Affairs, Office of Regulatory (2024-08-09). "FDA Bioresearch Monitoring Information". FDA. Retrieved 2025-05-15.
"1981 Questions & Answers - Good Laboratory Practice Regulations". U.S. Food and Drug Administration (published July 2007). 1981 [June 1981]. Archived from the original on June 12, 2019. Retrieved 12 April 2024.
"FDA - Health and Welfare Canada HPB, MOU on GLPs and Inspection Programs". U.S. Food and Drug Administration. 30 January 2018. Archived from the original on October 2, 2019. Retrieved 18 April 2024.
"FDA - France, MOU Regarding Collaboration and Cooperation". U.S. Food and Drug Administration. 30 January 2018. Retrieved 18 April 2024.
"FDA - Germany, MOU on Good Laboratory Practice". U.S. Food and Drug Administration. 31 January 2018. Retrieved 18 April 2024.
"FDA - Italy, MOU Regarding Safety Evaluation Data". U.S. Food and Drug Administration. 31 January 2018. Archived from the original on October 2, 2019. Retrieved 18 April 2024.
"FDA - Japan, GLP Mutual Recognition - Japanese Note Verbal". U.S. Food and Drug Administration. 31 January 2018. Archived from the original on October 2, 2019. Retrieved 18 April 2024.
"FDA - Netherlands, MOU Regarding Good Laboratory Practice". U.S. Food and Drug Administration. 31 January 2018. Archived from the original on October 2, 2019. Retrieved 18 April 2024.
"FDA - Sweden, MOU Regarding Good Laboratory Practice (GLP)". U.S. Food and Drug Administration. 31 January 2018. Retrieved 18 April 2024.
"FDA - Switzerland, MOU Regarding Good Laboratory Practice (GLP)". U.S. Food and Drug Administration. 31 January 2018. Retrieved 18 April 2024.
"Cooperative Arrangements". U.S. Food and Drug Administration. 23 February 2024. Retrieved 18 April 2024.
"Good Laboratory Practice for Nonclinical Laboratory Studies". U.S. Food and Drug Administration. March 26, 2018. Retrieved April 17, 2024.
"Comparison Chart of FDA and EPA Good Laboratory Practice (GLP) Regulations and the OECD Principles of GLP". FDA. November 3, 2018 – via www.fda.gov.^{[dead link]}
"Comparison Chart of FDA and EPA Good Laboratory Practice (GLP) Regulations and the OECD Principles of GLP". U.S. Food and Drug Administration. April 7, 2015 [June 2004]. Retrieved April 23, 2024.^{[dead link]}

accessdata.fda.gov

"CFR - Code of Federal Regulations Title 21". www.accessdata.fda.gov. Archived from the original on November 1, 2002. Retrieved 2024-04-12.

federalregister.gov

"Good Laboratory Practice for Nonclinical Laboratory Studies - A Proposed Rule by the Food and Drug Administration on 08/24/2016". Federal Register - The Daily Journal of the United States Government. 24 August 2016. Retrieved 17 April 2024.

govinfo.gov

"GOOD LABORATORY PRACTICE STANDARDS". www.govinfo.gov. Retrieved 2024-04-17.
"GOOD LABORATORY PRACTICE STANDARDS". www.govinfo.gov. Retrieved 2024-04-17.

hma.eu

"Question and Answer document on Good Laboratory Practice" (PDF). www.hma.eu.
"Question and Answer document on Good Laboratory Practice" (PDF). Heads of Medicines Agencies Clinical Trials Coordination Group. March 2017. Retrieved 18 April 2024.
"Heads of Medicines Agencies: Clinical Trials Coordination Group". www.hma.eu.
"Recommendation paper on principles of Good Laboratory Practices (GLP) for clinical trial applications under the EU Clinical Trials Regulation (Regulation (EU) No 536/2014)" (PDF). www.hma.eu.
"Recommendation paper on principles of Good Laboratory Practices (GLP) for clinical trial applications under the EU Clinical Trials Regulation (Regulation (EU) No 536/2014) Version 01" (PDF). Heads of Medicines Agencies Clinical Trials Coordination Group. March 2024. Retrieved 18 April 2024.
"Heads of Medicines Agencies: Clinical Trials Coordination Group". www.hma.eu. Retrieved 2024-04-18.

nih.gov

olaw.nih.gov

"MOU Among USDA/FDA/NIH | OLAW". olaw.nih.gov. Retrieved 2024-04-23.

oecd.org

"OECD SERIES ON PRINCIPLES OF GOOD LABORATORY PRACTICE AND COMPLIANCE MONITORING Number 1". Archived from the original on 2022-07-07.
"OECD Principles of Good Laboratory Practice (as revised in 1997)". OECD Environmental Health and Safety Publications. 1. OECD. 1998. Archived from the original on 20 April 2010. Retrieved 15 October 2006.
"OECD Principles of Good Laboratory Practice (GLP) and GLP Compliance Monitoring". Organisation for Economic Co-operation and Development. Retrieved April 28, 2024.
"Testing of chemicals". OECD.
"Mutual Acceptance of Data (MAD) - OECD". www.oecd.org. Archived from the original on 2022-01-20. Retrieved 2025-05-15.
"Mutual Acceptance of Data (MAD)". Organisation for Economic Co-operation and Development. Retrieved April 28, 2024.
"Omics technologies in chemical testing". OECD.
"COUNCIL DECISION AMENDING ANNEX II TO THE COUNCIL DECISION CONCERNING THE MUTUAL ACCEPTANCE OF DATA IN THE ASSESSMENT OF CHEMICALS [C(81)30(FINAL)]". www.oecd.org. Archived from the original on 2022-10-04.

planetwaves.net

Schneider, K (Spring 1983). "Faking it: The case against Industrial Bio-Test Laboratories". Amicus Journal. Natural Resources Defence Council: 14–26. Archived from the original on 14 February 2012. Retrieved 16 April 2011.

regulations.gov

"Regulations.gov". www.regulations.gov. Retrieved 2024-04-17.

web.archive.org

"OECD SERIES ON PRINCIPLES OF GOOD LABORATORY PRACTICE AND COMPLIANCE MONITORING Number 1". Archived from the original on 2022-07-07.
"OECD Principles of Good Laboratory Practice (as revised in 1997)". OECD Environmental Health and Safety Publications. 1. OECD. 1998. Archived from the original on 20 April 2010. Retrieved 15 October 2006.
Kevin Robinson for BioPharm International, 1 Aug 2003. GLPs and the Importance of Standard Operating Procedures Archived 21 March 2005 at the Wayback Machine
Schneider, K (Spring 1983). "Faking it: The case against Industrial Bio-Test Laboratories". Amicus Journal. Natural Resources Defence Council: 14–26. Archived from the original on 14 February 2012. Retrieved 16 April 2011.
"Good Laboratory Practice (GLP), Proposed Rule, 11/19/1976". U.S. Food and Drug Administration. December 22, 2020 [November 19, 1976]. Archived from the original on December 13, 2019. Retrieved April 23, 2024.
"Good Laboratory Practice Regulations Management Briefings Post Conference Report". U.S. Food and Drug Administration. February 24, 2020 [August 1979]. Archived from the original on September 30, 2020. Retrieved April 23, 2024.
"Good Laboratory Practice (GLP), Amendment, Final Rule, 9/4/1987". U.S. Food and Drug Administration. December 22, 2020 [September 4, 1987]. Archived from the original on December 13, 2019. Retrieved April 23, 2024.
Staff, World Health Organization (2009) Handbook: Good Laboratory Practice (GLP) Archived 9 February 2021 at the Wayback Machine
"CFR - Code of Federal Regulations Title 21". www.accessdata.fda.gov. Archived from the original on November 1, 2002. Retrieved 2024-04-12.
Commissioner, Office of the (2025-03-25). "Federal Food, Drug, and Cosmetic Act (FD&C Act)". FDA. Archived from the original on May 2, 2019. Retrieved 2025-05-15.
"Bioresearch Monitoring Program (BIMO) Compliance Program 7348.810 Sponsors and Contract Research Organizations". U.S. Food and Drug Administration. September 15, 2021. Archived from the original on December 14, 2019. Retrieved April 23, 2024.
"1981 Questions & Answers - Good Laboratory Practice Regulations". U.S. Food and Drug Administration (published July 2007). 1981 [June 1981]. Archived from the original on June 12, 2019. Retrieved 12 April 2024.
"FDA - Health and Welfare Canada HPB, MOU on GLPs and Inspection Programs". U.S. Food and Drug Administration. 30 January 2018. Archived from the original on October 2, 2019. Retrieved 18 April 2024.
"FDA - Italy, MOU Regarding Safety Evaluation Data". U.S. Food and Drug Administration. 31 January 2018. Archived from the original on October 2, 2019. Retrieved 18 April 2024.
"FDA - Japan, GLP Mutual Recognition - Japanese Note Verbal". U.S. Food and Drug Administration. 31 January 2018. Archived from the original on October 2, 2019. Retrieved 18 April 2024.
"FDA - Netherlands, MOU Regarding Good Laboratory Practice". U.S. Food and Drug Administration. 31 January 2018. Archived from the original on October 2, 2019. Retrieved 18 April 2024.
"Mutual Acceptance of Data (MAD) - OECD". www.oecd.org. Archived from the original on 2022-01-20. Retrieved 2025-05-15.
"COUNCIL DECISION AMENDING ANNEX II TO THE COUNCIL DECISION CONCERNING THE MUTUAL ACCEPTANCE OF DATA IN THE ASSESSMENT OF CHEMICALS [C(81)30(FINAL)]". www.oecd.org. Archived from the original on 2022-10-04.

who.int

Staff, World Health Organization (2009) Handbook: Good Laboratory Practice (GLP) Archived 9 February 2021 at the Wayback Machine

worldcat.org

search.worldcat.org

Baldeshwiler, Anne (29 July 2003). "History of FDA good laboratory practices". The Quality Assurance Journal. 7 (3): 157–161. doi:10.1002/qaj.228. eISSN 1099-1786. ISSN 1087-8378 – via Wiley Online Library.