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 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.

Medienart:

E-Artikel

Erscheinungsjahr:

2023

Erschienen:

2023

Enthalten in:

Zur Gesamtaufnahme - volume:15

Enthalten in:

Bioanalysis - 15(2023), 22 vom: 09. Nov., Seite 1381-1388

Sprache:

Englisch

Beteiligte Personen:

Tudan, Christopher [VerfasserIn]

Links:

Volltext

Themen:

Audits
CRO
Clinical
Confidentiality
Contract research organization
Data integrity
Fit-for-purpose
Informed consent
Journal Article
Protocol
Regulatory
Review
Sponsor

Anmerkungen:

Date Completed 01.11.2023

Date Revised 01.11.2023

published: Print-Electronic

Citation Status MEDLINE

doi:

10.4155/bio-2023-0150

funding:

Förderinstitution / Projekttitel:

PPN (Katalog-ID):

NLM362337160