Guidance for Industry Bioanalytical Method Validation Guidance for Industry Bioanalytical Method Validation

  • U.S. FDA
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Abstract

This draft guidance, when finalized, will represent the Food and Drug Administration’s (FDA’s) current thinking on this topic. It does not create or confer any rights for or on any person and does not operate to bind FDA or the public. You can use an alternative approach if the approach satisfies the requirements of the applicable statutes and regulations. If you want to discuss an alternative approach, contact the FDA staff responsible for implementing this guidance. If you cannot identify the appropriate FDA staff, call the appropriate number listed on the title page of this guidance.

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APA

U.S. FDA. (2018). Guidance for Industry Bioanalytical Method Validation Guidance for Industry Bioanalytical Method Validation. Bioanalytical Method Validation, (May), 1–41. Retrieved from https://cir.nii.ac.jp/crid/1571135650822060800%0Ahttp://www.fda.gov/downloads/drugs/guidancecomplianceregulatoryinformation/guidances/ucm368107.pdf

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