Prezzo Kindle: 48,74 €

Risparmia 20,89 € (30%)

Il prezzo include l’IVA

Al momento dell'acquisto potrebbero essere applicate delle promozioni

Queste promozioni verranno applicate al seguente articolo:

Alcune promozioni sono cumulabili; altre non possono essere unite con ulteriori promozioni. Per maggiori dettagli, vai ai Termini & Condizioni delle specifiche promozioni.

Leggilo con la nostra App gratuita
Ti sei abbonato a ! Preordineremo i tuoi articoli entro 24 ore dalla data in cui saranno disponibili. Non appena vengono rilasciati nuovi libri, addebiteremo sul tuo metodo di pagamento predefinito il prezzo più basso disponibile durante il periodo di preordine.
Aggiorna il dispositivo o il metodo di pagamento, annulla i singoli preordini o l'abbonamento da
I tuoi abbonamenti

Acquista per altri

Regala questo eBook o acquista per un gruppo.
Ulteriori informazioni

Acquista e invia eBook ad altri

  1. Seleziona quantità
  2. Seleziona una modalità di invio e completa l'acquisto
  3. I destinatari possono leggere gli eBook su qualsiasi dispositivo

Questi eBook possono essere riscattati esclusivamente da destinatari residenti nel tuo Paese. I link di riscatto e gli eBook non possono essere rivenduti o trasferiti.
Immagine del logo dell'app Kindle

Scarica l'app Kindle gratuita e inizia a leggere immediatamente i libri Kindle sul tuo smartphone, tablet o computer, senza bisogno di un dispositivo Kindle.

Leggi immediatamente sul browser con Kindle per il Web.

Con la fotocamera del cellulare scansiona il codice di seguito e scarica l'app Kindle.

Codice QR per scaricare l'app Kindle

Segui l'autore

Rick Ng
+ Segui
Altri libri di questo autore
Si è verificato un errore. Riprova a effettuare la richiesta più tardi.

Drugs: From Discovery to Approval (English Edition) 1° Edizione, Formato Kindle

Edizione Inglese di Rick Ng (Autore) Formato: Formato Kindle
4,7 4,7 su 5 stelle 69 voti
Visualizza tutti i formati ed edizioni
Statistics show that out of five thousand compounds with initial promise, five will go into human clinical trials, and only one will become an approved drug. This tiny fraction illustrates the huge complexities involved in bringing a drug to market, a process that brings together scientific research, medical ethics, business, and various regulatory agencies.
Drugs-From Discovery to Approval presents a clear, step-by-step overview of the entire process. Using simple language, this comprehensive guide introduces basic concepts, then moves on to discuss disease target selection and the discovery processes for both small and large molecule drugs. Subsequent chapters explain preclinical studies, clinical trials, regulatory issues, good manufacturing practices (GMPs), and perspectives on the future. Coverage also includes:
* A helpful listing of current FDA and European guidelines
* A special section on regulatory authorities and processes in Japan and China
* Rich illustrations throughout, including more than ninety figures and tables
* Useful appendices on the history of drug discovery and development
* Representative examples of drug mechanisms in action
Written for professionals in the pharmaceutical industry, and readily accessible for students of pharmacy or medicine and others interested in drug discovery, Drugs-From Discovery to Approval represents a practical and approachable reference on this important process.
Leggi di più Leggi meno
Previous page
  1. ISBN-13
    978-0471601500
  2. Edizione
    1°
  3. Memo
    Su Kindle Scribe
  4. Editore
    Wiley-Liss
  5. Data di pubblicazione
    2 maggio 2008
  6. Lingua
    Inglese
  7. Dimensioni file
    15200 KB
  8. Visualizza tutti i dettagli
Next page
A causa delle dimensioni del file, il download di questo libro potrebbe richiedere più tempo.
Amazon Original Books
eBook thriller, romanzi gialli, romanzi rosa, narrativa storica e tanti altri generi in esclusiva a meno di 5 EUR Clicca qui

Chi ha acquistato questo articolo ha acquistato anche

Pagina 1 di 1 RicominciaPagina 1 di 1
Previous page
  1. Drug Discovery and Development E-Book (English Edition)
Next page

Descrizione prodotto

Dalla seconda/terza di copertina

The third edition of this best-selling book continues to offer a user-friendly, step-by-step introduction to all the key processes involved in bringing a drug to the market, including the performance of pre-clinical studies, the conduct of human clinical trials, regulatory controls, and even the manufacturing processes for pharmaceutical products.

Concise and easy to read, Drugs: From Discovery to Approval, Third Edition quickly introduces basic concepts and then moves on to discuss target selection and the drug discovery process for both small and large molecular drugs. The third edition incorporates the latest developments and updates in the pharmaceutical community, provides more comprehensive coverage of topics, and includes more materials and case studies suited to college and university use. Biotechnology is a dynamic field with changes across R&D, clinical trials, manufacturing, and regulatory processes; the third edition of the text provides timely updates for those in this rapidly growing field.

* Revised edition will have greater appeal to students with the inclusion of more materials and case studies suited to college and university use

* Includes the latest developments and updates

* Increased appeal by provision of more comprehensive topics

Dalla quarta di copertina

Statistics show that out of five thousand compounds with initial promise, five will go into human clinical trials, and only one will become an approved drug. This tiny fraction illustrates the huge complexities involved in bringing a drug to market, a process that brings together scientific research, medical ethics, business, and various regulatory agencies.

Drugs?From Discovery to Approval presents a clear, step-by-step overview of the entire process. Using simple language, this comprehensive guide introduces basic concepts, then moves on to discuss disease target selection and the discovery processes for both small and large molecule drugs. Subsequent chapters explain preclinical studies, clinical trials, regulatory issues, good manufacturing practices (GMPs), and perspectives on the future. Coverage also includes:

  • A helpful listing of current FDA and European guidelines
  • A special section on regulatory authorities and processes in Japan and China
  • Rich illustrations throughout, including more than ninety figures and tables
  • Useful appendices on the history of drug discovery and development
  • Representative examples of drug mechanisms in action

Written for professionals in the pharmaceutical industry, and readily accessible for students of pharmacy or medicine and others interested in drug discovery, Drugs?From Discovery to Approval represents a practical and approachable reference on this important process.

Dettagli prodotto

  • ASIN ‏ : ‎ B003772KD8
  • Editore ‏ : ‎ Wiley-Liss; 1° edizione (2 maggio 2008)
  • Lingua ‏ : ‎ Inglese
  • Dimensioni file ‏ : ‎ 15200 KB
  • Da testo a voce ‏ : ‎ Abilitato
  • Screen Reader ‏ : ‎ Supportato
  • Miglioramenti tipografici ‏ : ‎ Abilitato
  • X-Ray ‏ : ‎ Non abilitato
  • Word Wise ‏ : ‎ Non abilitato
  • Memo ‏ : ‎ Su Kindle Scribe
  • Lunghezza stampa ‏ : ‎ 368 pagine
  • Recensioni dei clienti:
    4,7 4,7 su 5 stelle 69 voti

Informazioni sull'autore

Segui gli autori per ottenere aggiornamenti sulle nuove uscite, oltre a consigli avanzati.
Rick Ng

Rick Ng

Brief content visible, double tap to read full content.
Full content visible, double tap to read brief content.

Scopri di più sui libri dell'autore, guarda autori simili, leggi i blog dell’autore e altro ancora

Recensioni clienti

4,7 su 5 stelle
4,7 su 5
69 valutazioni globali

Recensioni migliori da Italia

Ci sono 0 recensioni e 0 valutazioni dall'Italia

Le recensioni migliori da altri paesi

Traduci tutte le recensioni in Italiano
sl
5,0 su 5 stelle excellent reference
Recensito negli Stati Uniti il 30 novembre 2023
Acquisto verificato
This book is practical and, yet, well updated on the topics. It presents the subjects clear and interesting. Not only a beginner but also an experienced professional would find it useful.
Segnala
Rutik Thorat
4,0 su 5 stelle Must read
Recensito in India il 9 dicembre 2020
Acquisto verificato
Little old version but has covered up important concepts and case studies in an excellent language
Segnala
Felipe Albrecht
4,0 su 5 stelle Good overview for newcomers in the pharmaceutical world.
Recensito in Germania il 16 novembre 2018
Acquisto verificato
Good overview for newcomers in the pharmaceutical world.
Segnala
Gaffboat
5,0 su 5 stelle An easy way to understand a complex process
Recensito negli Stati Uniti il 21 agosto 2006
Acquisto verificato
I work in an organization that supports advanced gene therapy research that may lead to new therapies for chronic and life threatening diseases, but I am not a scientist. As a communicator, I needed to understand the long and arduous journey from discovery to pre-clinical research, to FDA-approved clinical manufacturing, and to human clinical trials. This book was excellent in helping me understand both the research and the regulatory environment.

The author says it best in the introduction, "The intention of this book is to provide an overview about how a drug is discovered, the amount of and types of laboratory tests that are performed, and the conduct of clinical trials before a drug is ready to registered for human use." The author also fully explains the role of regulatory authorities in these processes.

The book includes chapters on:

Drug discovery

Drug development and preclinical studies

Clinical trials

Good Manufacturing Practice

You'll also learn about things like toxicology studies, pharmacodynamics, and pharmacokinetics, and Investigational New Drug applications. Although the book contains some technical discussions and exhibits, the author has a logical and easy-to-understand way of presenting the information.

If, like me, you need to get a better understanding of process of getting basic drug research to the market, this book is for you.
13 persone l'hanno trovato utile
 Segnala
Jonathan M. Lourie
4,0 su 5 stelle Good Overview of Drug Approval Process
Recensito negli Stati Uniti il 4 aprile 2005
Acquisto verificato
This book fills a needed hole in the books about the pharma/drug industry. It provides a concise review of the drugs from discovery to approval and details the various steps along the way, including discovery, clinical trials, manfacturing and approval. There is enough science to provide the necessary background but not so much that the non scientist would be overwhelmed. It is well illustrated with plenty of diagrams and outlines. Dr. Ng delivers on a summary which can be read by novice to intermediate who desires to know more about the process. I think this book is a must read for attorneys or business people who are looking to understand the drug approval process and are working in the industry. It is also up to date which is very important in this field, where regulations can change. Finally it covers both US and other countries, although its US coverage is better than its non US coverage. This is the only reason I did not give the book 5 stars.

I find this book a good personal reference in a short concise form and therefore recommend it.
22 persone l'hanno trovato utile
 Segnala
Segnala un problema

Questo articolo ha contenuti inappropriati?
Segnala
Credi che questo articolo violi un copyright?
Segnala
In questo articolo sono presenti problemi di qualità o di formattazione?
Segnala