
Download App
>> | LShop | >> | Book | >> | Medicine | >> | Medical Study & Revi... | >> | Pharmaceutical Toxic... |
ISBN
:
9780470371374
Publisher
:
John Wiley & Sons
Subject
:
Medical Study & Revision Guides & Reference Material
Binding
:
Hardcover
Pages
:
258
Year
:
202
₹
10829.0
₹
10829.0
Buy Now
Shipping charges are applicable for books below Rs. 101.0
View DetailsEstimated Shipping Time : 5-7 Business Days
View DetailsDescription
This book describes, with references to key source materials, the background to, and conduct of, the principal nonclinical studies that are central to drug development. The chapters provide an understanding of the key components of the preclinical phase of drug development with a hands-on description, with core chapters addressing study conduct, types, and reporting. As such, it is a practical guide through toxicology testing and an up-to-date reference on current issues, new developments, and future directions in toxicology. Opening with a practical description of toxicology and its role in the development of pharmaceuticals, the book proceeds to detail international regulations (including the impact of the new REACH standards for chemical safety), interdisciplinary interactions among scientists in drug development, steps in toxicity testing, and risk management. Further, the book covers the methods of genetic toxicology (assays, genomics, in vivo screening) as a complement to “traditional” toxicology in the risk assessment and risk management of pharmaceuticals.
Author Biography
ALBERTO LODOLA is a consulting toxicologist at ToxAdvantage. Prior to this, he spent twenty years at Pfizer, where he became the senior director and head of the toxicology department for the Amboise, France, laboratory. Dr. Lodola has published over forty peer-reviewed papers since 1974.JEANNE STADLER is an independent consulting toxicologist, following a thirty-four year career at Pfizer R&D, in Amboise, France, coming from the toxicology department and rising to the level of scientific advisor and director. She is the coeditor of one book and the author of forty peer-reviewed papers. Dr. Stadler continues to be a regular speaker and training session leader at professional meetings and at universities.
Related Items
-
of
Pharmaceutical Water: System Design, Operation, and Validation
William V. Collentro
Starts At
21004.0
27637.0
24% OFF
Pharmaceutical Master Validation Plan: The Ultimate Guide To FDA,GMP, & GIP Compliance, With CD-Rom
Syed Imtiaz Haider
Starts At
3435.0
3995.0
14% OFF
A Textbook Of Pharmaceutical Analysis, 3Rd Ed
Kenneth A. Connors
Starts At
1089.0
1329.0
18% OFF
Practice-Based Learning and Improvement: A Clinical Improvement Action Guide
Eugene C. Nelson
Starts At
4542.0
6398.0
29% OFF
Ansel's Pharmaceutical Dosage Forms And Drug Delivery Systems, 8E
Wolters
Starts At
630.0
875.0
28% OFF
BENTLEY AND DRIVERS TEXTBOOK OF PHARMACEUTICAL CHEMISTRY 8ED
BENTLEY
Starts At
413.0
530.0
22% OFF
Immunization in Practice: A Practical Guide for Health Staff
B. Sridhar Rao
Starts At
108.0
125.0
13% OFF
Martins Physical Pharmacy And Pharmaceutical Sciences,5/e
Sinko
Starts At
860.0
1195.0
28% OFF
Process Chemistry in the Pharmaceutical Industry
Kumar G. Gadamasetti
Starts At
2830.0
3495.0
19% OFF
Handbook of Non-Invasive Drug Delivery Systems: Non-Invasive and Minimally-Invasive Drug Delivery Systems for Pharmaceutical and Personal Care Product
Kulkarni Vitthal S.
Starts At
20540.0
23884.0
14% OFF
Are you sure you want to remove the item from your Bag?
Yes
No
Added to Your Wish List
OK
Your Shopping Bag
- 2 Items
Item
Delivery
Unit Price
Quantity
Sub Total
Order Summary