Demonstrating Results Equivalence of Bacterial Endotoxins Test Methods.


Journal

PDA journal of pharmaceutical science and technology
ISSN: 1948-2124
Titre abrégé: PDA J Pharm Sci Technol
Pays: United States
ID NLM: 9439538

Informations de publication

Date de publication:
23 Aug 2024
Historique:
medline: 24 8 2024
pubmed: 24 8 2024
entrez: 23 8 2024
Statut: epublish

Résumé

The LAL test has been the "gold standard" for endotoxin testing ever since it was first published as USP Chapter <85> in 1980. Since then, a number of innovative methods have been proposed to augment or replace the LAL test. However novel an alternate test method might be, we must be cognizant of our obligation to patient safety and heed compendial and compliance requirements to demonstrate results equivalence between any candidate (alternate) method and a predicate (compendial) test method. The following discussion explores the concepts of "equivalent", "different" and "not different", proposes the use of a two one sided test (TOST) for the demonstration of equivalence and provides examples of calculations using commercially available software to assess data on alternative endotoxins detection methods that have been published in the public domain1.

Identifiants

pubmed: 39179395
pii: pdajpst.2023.012871
doi: 10.5731/pdajpst.2023.012871
doi:

Substances chimiques

Endotoxins 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

501-511

Informations de copyright

© PDA, Inc. 2024.

Auteurs

Steven Walfish (S)

Statistical Outsourcing Services, Rockville, MD; steven@statisticaloutsourcingservices.com.

John Duguid (J)

Research & Development, Vericel Corporation; and.

Karen McCullough (K)

MMI Associates, LLC.

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Classifications MeSH