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This technical report presents the recommendations of a group of international experts convened by the World Health Organization to discuss quality assurance of pharmaceuticals, specifications for
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01
Obtain the WHO Technical Report Series 908 from the WHO website or other authorized sources.
02
Read the introductory section to understand the overall purpose of the report.
03
Review the contents section to familiarize yourself with the structure of the report.
04
Identify the specific sections that pertain to your area of interest or research.
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Fill out necessary details in any forms or templates provided within the report.
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Ensure all data is accurate and relevant to the guidelines established in the report.
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Submit the filled report to the relevant authority or organization as instructed.

Who needs WHO Technical Report Series 908?

01
Healthcare professionals and researchers working in public health.
02
Regulatory agencies involved in health-related policies.
03
Pharmaceutical and biotechnological companies developing new medical products.
04
Academic institutions conducting health-related research.
05
Global health organizations looking for standardized guidelines.
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WHO Expert Committee on Specifications for Pharmaceutical Preparations - TRS 1044. The Expert Committee on Specifications for Pharmaceutical Preparations works towards clear, independent and practical standards and guidelines for the quality assurance of medicines and provision of global regulatory tools.
This document provides guidance for quality management systems within pharmaceutical quality control laboratories. It aims to help laboratories obtain accurate and reliable test results, promote harmonization, and facilitate mutual recognition of results.
WHO Technical Report Series WHO PREQUALIFICATION REQUIREMENTS FOR VACCINES. CLINICAL EVALUATION OF VACCINES. LOT RELEASE OF VACCINES. NONCLINICAL EVALUATION OF VACCINES. REGULATION AND QUALITY CONTROL OF VACCINES. REGULATORY EXPECTATIONS FOR THIOMERSAL-CONTAINING VACCINES. REGULATION OF POST-APPROVAL CHANGES TO VACCINES.
The WHO Technical Report Series (TRS) makes available the findings of various international groups of experts that provide WHO with the latest scientific and technical advice on a broad range of medical and public health subjects.

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WHO Technical Report Series 908 is a publication by the World Health Organization that provides guidelines and recommendations for the quality control and testing of biological and pharmaceutical products.
Regulatory authorities, manufacturers of biological and pharmaceutical products, and other stakeholders involved in the production and quality control of these products are required to refer to and align with the guidelines stated in WHO Technical Report Series 908.
To fill out WHO Technical Report Series 908, organizations must follow the specific guidelines provided in the document, which include detailed instructions on the format, necessary data, and any additional documentation required for submission.
The purpose of WHO Technical Report Series 908 is to ensure the safety, efficacy, and quality of biological and pharmaceutical products through standardized practices and rigorous testing criteria.
The information that must be reported includes data on product characteristics, manufacturing processes, quality control measures, testing results, and any deviations or issues encountered during production.
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