Vi bøger
Levering: 1 - 2 hverdage
Forlænget returret til d. 31. januar 2025

The Certified Pharmaceutical GMP Professional Handbook - Mark Allen Durivage - Bog

Bag om The Certified Pharmaceutical GMP Professional Handbook

The purpose of this handbook is to assist individuals for the Certified Pharmaceutical Good Manufacturing Practices Professional (CPGP) examination and provide a reference for the practitioner. The second edition reflects the Body of Knowledge which was updated in 2015. This edition has also incorporated additional information including updated references. The updates reflect the current trends and expectations of the evolving pharmaceutical industry driven by consumer expectations and regulatory oversight. This handbook covers compliance with good manufacturing practices (GMPs), as regulated and guided by national and international agencies for the pharmaceutical industry. It covers finished human and veterinary drugs and biologics, and combination devices, as well as their component raw materials (including active pharmaceutical ingredients (APIs) and excipients), and packaging and labeling operations.

Vis mere
  • Sprog:
  • Engelsk
  • ISBN:
  • 9780873899338
  • Indbinding:
  • Hardback
  • Sideantal:
  • 514
  • Udgivet:
  • 23. maj 2016
  • Udgave:
  • 16002
  • Størrelse:
  • 183x32x260 mm.
  • Vægt:
  • 1154 g.
  • 2-4 uger.
  • 11. januar 2025
På lager
Forlænget returret til d. 31. januar 2025
  •  

    Kan ikke leveres inden jul.
    Køb nu og print et gavebevis

Normalpris

Medlemspris

Prøv i 30 dage for 45 kr.
Herefter fra 79 kr./md. Ingen binding.

Beskrivelse af The Certified Pharmaceutical GMP Professional Handbook

The purpose of this handbook is to assist individuals for the Certified Pharmaceutical Good Manufacturing Practices Professional (CPGP) examination and provide a reference for the practitioner. The second edition reflects the Body of Knowledge which was updated in 2015. This edition has also incorporated additional information including updated references. The updates reflect the current trends and expectations of the evolving pharmaceutical industry driven by consumer expectations and regulatory oversight.
This handbook covers compliance with good manufacturing practices (GMPs), as regulated and guided by national and international agencies for the pharmaceutical industry. It covers finished human and veterinary drugs and biologics, and combination devices, as well as their component raw materials (including active pharmaceutical ingredients (APIs) and excipients), and packaging and labeling operations.

Brugerbedømmelser af The Certified Pharmaceutical GMP Professional Handbook



Find lignende bøger
Bogen The Certified Pharmaceutical GMP Professional Handbook findes i følgende kategorier:

Gør som tusindvis af andre bogelskere

Tilmeld dig nyhedsbrevet og få gode tilbud og inspiration til din næste læsning.