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Controversy over genetically modified organisms: the governing laws and regulations.
Qual Assur. 2000 Jan-Mar;8(1):33-6. doi: 10.1080/105294100753209174.
Qual Assur. 2000.
PMID: 11710306
A comparison of the U.S. EPA FIFRA GLP standards with the U.S. FDA GLP standards for nonclinical laboratory studies.
Keatley KL.
Keatley KL.
Qual Assur. 1999 Jul-Sep;7(3):147-54. doi: 10.1080/105294100750035125.
Qual Assur. 1999.
PMID: 11033740
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A review of US EPA and FDA requirements for electronic records, electronic signatures, and electronic submissions.
Keatley KL.
Keatley KL.
Qual Assur. 1999 Apr-Jun;7(2):77-89. doi: 10.1080/10529410050133844.
Qual Assur. 1999.
PMID: 10992873
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A review of the FDA draft guidance document for software validation: guidance for industry.
Keatley KL.
Keatley KL.
Qual Assur. 1999;7(1):49-55. doi: 10.1080/105294100277723.
Qual Assur. 1999.
PMID: 10707376
Review.
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Good Laboratory Practice in the Academic Setting: Fundamental Principles for Nonclinical Safety Assessment and GLP-Compliant Pathology Support When Developing Innovative Biomedical Products.
Bolon B, Baze W, Shilling CJ, Keatley KL, Patrick DJ, Schafer KA.
Bolon B, et al. Among authors: keatley kl.
ILAR J. 2018 Dec 1;59(1):18-28. doi: 10.1093/ilar/ily008.
ILAR J. 2018.
PMID: 30566589
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