Good clinical practices in the bioanalytical laboratory

Despite the existence of good clinical practice guidelines, the way in which they are applied to the bioanalytical laboratory remains unclear. Aspects of patient confidentiality, informed consent and subject withdrawal; addressing unblinding associated with sample analysis, including repeat analysis...

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Published inBioanalysis Vol. 15; no. 22; pp. 1381 - 1388
Main Author Tudan, Christopher
Format Journal Article
LanguageEnglish
Published Newlands Press Ltd 01.11.2023
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ISSN1757-6180
1757-6199
DOI10.4155/bio-2023-0150

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Abstract Despite the existence of good clinical practice guidelines, the way in which they are applied to the bioanalytical laboratory remains unclear. Aspects of patient confidentiality, informed consent and subject withdrawal; addressing unblinding associated with sample analysis, including repeat analysis and incurred sample reanalysis; or the differences in responsibilities between the sponsor and contract research organization are not articulated by the US FDA within the bioanalytical setting, and for most bioanalytical laboratories this remains a gap in their standard operating procedures. The aim of this article is to identify and clarify the aspects of the good clinical practices that are applicable to the bioanalytical laboratory when conducting bioanalysis with clinical samples, and to address potential gaps in the bioanalytical laboratory when it comes to clinical sample bioanalysis.
AbstractList Despite the existence of good clinical practice guidelines, the way in which they are applied to the bioanalytical laboratory remains unclear. Aspects of patient confidentiality, informed consent and subject withdrawal; addressing unblinding associated with sample analysis, including repeat analysis and incurred sample reanalysis; or the differences in responsibilities between the sponsor and contract research organization are not articulated by the US FDA within the bioanalytical setting, and for most bioanalytical laboratories this remains a gap in their standard operating procedures. The aim of this article is to identify and clarify the aspects of the good clinical practices that are applicable to the bioanalytical laboratory when conducting bioanalysis with clinical samples, and to address potential gaps in the bioanalytical laboratory when it comes to clinical sample bioanalysis.
Author Tudan, Christopher
AuthorAffiliation 1Veloxity Labs, 801 W Main St, Peoria, IL 61606, USA
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10.1007/s11095-005-9045-3
10.4155/bio-2021-0046
10.4155/bio.15.11
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Snippet Despite the existence of good clinical practice guidelines, the way in which they are applied to the bioanalytical laboratory remains unclear. Aspects of...
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StartPage 1381
SubjectTerms audits
clinical
confidentiality
contract research organization
CRO
data integrity
fit-for-purpose
informed consent
protocol
regulatory
sponsor
Title Good clinical practices in the bioanalytical laboratory
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