An insight into the presence of impurities in reference standards and their impact on mass spectrometry-based bioanalysis

Author:

Ghoghari Ashok M1ORCID,Patel Harilal V1,Jain Mukul R1

Affiliation:

1. Bioanalytical Laboratory, Zydus Research Center, Ahmedabad, 382210, Gujarat, India

Publisher

Future Science Ltd

Subject

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

Reference7 articles.

1. Metabolites in safety testing

2. ICH. ICH harmonized guideline: bioanalytical method validation and study sample analysis, M10 (2022).

3. US Pharmacopeia. USP chapters <1086> impurities in drug substances and drug products. In:USP 41. US Pharmacopeial Convention, MD, USA (2018).

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