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B01=Andrew Teasdale
B01=David Elder
B01=Raymond W. Nims
Category1=Non-Fiction
Category=PN
Category=TDCW
COP=United States
Delivery_Delivery within 10-20 working days
Language_English
PA=Available
Price_€100 and above
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ICH Quality Guidelines: An Implementation Guide

English

Examining the implications and practical implementation of multi-disciplinary International Conference on Harmonization (ICH) topics, this book gives an integrated view of how the guidelines inform drug development strategic planning and decision-making.

    Addresses a consistent need for interpretation, training, and implementation examples of ICH guidelines via case studies
    Offers a primary reference point for practitioners addressing the dual challenge of interpretation and practical implementation of ICH guidelines
    Uses case studies to help readers understand and apply ICH guidelines
    Provides valuable insights into guidelines development, with chapters by authors involved in generating or with experience implementing the guidelines
    Includes coverage of stability testing, analytical method validation, impurities, biotechnology drugs and products, and good manufacturing practice (GMP) See more
Current price €286.89
Original price €301.99
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Age Group_Uncategorizedautomatic-updateB01=Andrew TeasdaleB01=David ElderB01=Raymond W. NimsCategory1=Non-FictionCategory=PNCategory=TDCWCOP=United StatesDelivery_Delivery within 10-20 working daysLanguage_EnglishPA=AvailablePrice_€100 and abovePS=Activesoftlaunch
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Product Details
  • Weight: 1225g
  • Dimensions: 158 x 234mm
  • Publication Date: 15 Dec 2017
  • Publisher: John Wiley & Sons Inc
  • Publication City/Country: United States
  • Language: English
  • ISBN13: 9781118971116

About

Andrew Teasdale PhD is a principal scientist in pharmaceutical development with AstraZeneca. He has over 20 years' experience within the industry and has held a number of leadership roles both internally and externally at a cross industry level encompassing key ICH topic areas. David Elder PhD is an independent CMC consultant. He has 40 years' experience within the pharmaceutical industry. He was formerly a director within GlaxoSmithKline's platform technology and science function. He is an expert member for the British Pharmacopoeia and has extensive CMC experience encompassing many of the key ICH topics. Raymond W. Nims PhD is a Senior Consultant at RMC Pharmaceutical Solutions with experience in a variety of GMP quality assurance and quality control topics from a biologics point of reference. He has served on ad hoc panels supporting a number of USP chapters and ANSI Standards.

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