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Analytical Testing For The Pharmaceutical GMP Laboratory (Original PDF From Publisher)
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Analytical Testing For The Pharmaceutical GMP Laboratory (EPUB)
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Analytical Testing For The Pharmaceutical GMP Laboratory (Original PDF From Publisher)

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Product Details

  • Publisher : Wiley; March 29, 2022
  • Language : English
  • ISBN : 9781119120919
  • ISBN : 9781119680468
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Description

Analytical Testing For The Pharmaceutical GMP Laboratory (Original PDF From Publisher)

Written by Kim Huynh-Ba

offers helpful advice on pharmacological analysis authored by eminent professionals with a wealth of knowledge in the field.

The comprehensive overview of pharmaceutical laws, operational procedures and best practices for drug development that are

employed to preserve the purity and quality of medications is provided by Analytical Testing for the Pharmaceutical GMP Laboratory.

The book offers the information required for setting up a pharmaceutical laboratory to support Quality Systems and adhere to

Good Manufacturing Practices (GMP) laws, with an emphasis on lower molecular weight medicinal ingredients and products.

Up-to-date information on drug legislation, pharmaceutical analysis methodology, control strategies, testing development and

validation, method transfer, electronic data documentation and more is covered in concise yet thorough chapters.

A table of contents, acronym definitions, a reference list and several tables and figures are included in every chapter.

This reputable site discusses the main tasks and legal issues associated with analytical testing in the creation and production of

pharmaceutical medicinal products.

outlines the GMP regulations, key guidelines, duties and organizational structure of the ICH and FDA. includes examples of

analytical procedures used for drug release and stability testing, as well as a discussion of common analytical technology utilized

in pharmaceutical laboratories. investigates control tactics developed from quality systems and backed by case studies from the

actual world.

explains the application of dissolution testing to goods including inhalers, aerosols and extended-release capsules.

explains stability programs, the Laboratory Information Management System (LIMS) and appropriate documentation and data

reporting techniques in order to maintain compliance.

In order to help readers with day-to-day laboratory activities, this section includes calculations, application examples, and pictures.

Provides useful information and templates for organizing standard operating procedures (SOPs) or internal operations.

Pharmaceutical scientists, analytical chemists, pharmacists, and quality control specialists in their early and advanced careers should

all own Analytical Testing for the Pharmaceutical GMP Laboratory.

It is also a great textbook for analytical chemistry courses taken at the undergraduate and graduate levels in the pharmaceutical

sciences or in regulatory compliance programs.

It is a resource for GMP laboratory training programs.

See Also : Analytical Testing For The Pharmaceutical GMP Laboratory (EPUB)

Additional information
Publisher

Wiley – Blackwell

Language

English

Edition

1

Format

Publisher PDF

File Size

6.1 MB

Publication Date

March 29, 2022

ISBN-13

9781119120919, 9781119680437, 9781119680468

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