EBF recommendation on practical management of critical reagents for PK ligand-binding assays

Author:

Pihl Susanne1,van der Strate Barry WA2,Golob Michaela3,Vermet Laurent4,Jaitner Birgit5,Goodman Joanne6,Fjording Marianne Scheel7,Timmerman Philip8

Affiliation:

1. Susanne Pihl, Ascendis Pharma A/S, Copenhagen, Denmark

2. PRA Health Sciences, Assen, The Netherlands

3. Nuvisan GmbH, Grafing, Germany

4. Sanofi Research & Development, Montpellier, France

5. Novartis Pharma AG, Basel, Switzerland

6. MedImmune, Cambridge, UK

7. Novo Nordisk A/S, Måløv, Denmark

8. European Bioanalysis Forum, Havenlaan 86c b204, 1000 Brussels, Belgium

Abstract

Critical reagents play a crucial role in ligand-binding assays; the robustness and reliability of an assay is defined by the quality and long-term availability of these reagents. However, neither regulatory guidelines nor relevant scientific papers provide clear directions for set-up, life cycle management and, more importantly, the acceptance criteria required for the testing of the critical reagents for pharmacokinetic, biomarker and immunogenicity assays. The ambiguity from current guidelines can be a challenge for the bioanalytical community. Members of the European Bioanalysis Forum community undertook a more pragmatic approach on how to assess the impact of critical reagents. In this paper, a review and corresponding gap analysis of the current guidelines and relevant papers will be provided as well as decision trees proposed for lot-to-lot changes of critical reagents for pharmacokinetic assays.

Publisher

Future Science Ltd

Subject

Medical Laboratory Technology,Clinical Biochemistry,General Pharmacology, Toxicology and Pharmaceutics,General Medicine,Analytical Chemistry

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