SN/T 4924-2017 in English

VALID

Determination of tetracyclines in edible animals for import and export-Radio-receptor assay

Issued on:2017-11-07
Implemented on:2018-06-01
File Format:PDF
Delivery:Via email within 1~3 business days

Price(USD)： $120.00
$117.00

Standard No:	SN/T 4924-2017
Document status:	VALID
Title in English:	Determination of tetracyclines in edible animals for import and export-Radio-receptor assay
Title in Chinese:	进出口食用动物中四环素类药物残留量的测定放射受体分析法
Language:	English
File Format:	Electronic (PDF)
Delivery:	Via email within 1~3 business days
Issued on:	2017-11-07
Implemented on:	2018-06-01
Professional Classification:	SN-Import&Export Inspection
Related Keywords:	edible animals export-radio-receptor assay introductionthis standard animals edible import
Related Topics:	volume analysis In Vivo Drug Analysis imported drugs in drug analysis Four Quantitative Analysis Methods receptor type IV radioreceptor method export food Residues of progesterone drugs in food of animal origin for import and export Drug Quantitative Analyzer drug analysis drug analysis Drug Analysis 3Q Chinese medicine in food Is there an antidote to tetracyclines? Drug target co-localization analysis Quantitative analysis methods in pharmaceutical analysis Determination method of tetracycline in water Cyclosporine Analytical Methods Pharmacopoeia Drug analysis methods for specific drugs Commonly used analytical methods for drug residue detection Common methods and characteristics of in vivo drug analysis Drug Quantitative Analysis Methods Commonly used methods for in vivo drug analysis Commonly used identification methods in in vivo drug analysis sn/t 4953-2017 Commonly used separation methods in pharmaceutical analysis sn/t 4972-2017 sn/t 4921-2017

Introduction

This standard provides a method for the determination of tetracycline residues in edible animals used for import and export. The method described is based on radioimmunoassay techniques. It outlines the procedures for sample preparation, extraction, and analysis to ensure accurate and reliable results. The standard specifies the equipment, reagents, and operational conditions required for the test. It also includes guidelines for the interpretation of results and the calculation of residue levels. The document is structured to facilitate the implementation of the method in laboratory settings. It covers key aspects such as calibration, quality control, and data reporting. The standard aims to ensure consistency and precision in the testing process.

*** Please note: This description may not be accurate, please refer to the official documentation.

More samples: DL/T 5154-2012 JJG 21-2008 QC/T 942-2021

Sample only — not a preview of SN/T 4924-2017

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