Jeanne Stadler (24 results)

Soft cover. Condition: Good. Softcover; minor edge notations in pencil; light foxing of wraps and edges; o/w in good condition. Book.

Soft Cover. Condition: Good. Wraps lightly tanning, edges rubbed. Small amount of markings in text. Bookplate on fep. Size: 8vo - over 7¾" - 9¾" tall. Ex Libris.

Paperback. Condition: Good. null. This hardcover edition of "Premiers Textes littéraires" is in good condition with some minor wear consistent with age. The cover features a notable illustration by Dan Nevins, and the spine remains intact. There is no dust jacket present, and the book does not contain any inscriptions or library markings. Overall, the binding is solid, and the pages are clean. ##.…

Condition: New. pp. vi + 258 Illus.

Condition: New. pp. vi + 258 Index.

hardcover. Condition: Good. Connecting readers with great books since 1972! Used textbooks may not include companion materials such as access codes, etc. May have some wear or writing/highlighting. We ship orders daily and Customer Service is our top priority.

Hardcover. Condition: Good. No Jacket. Pages can have notes/highlighting. Spine may show signs of wear. ~ ThriftBooks: Read More, Spend Less.

Condition: Brand New. New. US edition. Expediting shipping for all USA and Europe orders excluding PO Box. Excellent Customer Service.

Condition: New. This is a Brand-new US Edition. This Item may be shipped from US or any other country as we have multiple locations worldwide.

Condition: Brand New. New. US edition. Expediting shipping for all USA and Europe orders excluding PO Box. Excellent Customer Service.

Condition: New. This is a Brand-new US Edition. This Item may be shipped from US or any other country as we have multiple locations worldwide.

Condition: New.

Condition: New. Brand New.

Condition: New. pp. vi + 258.

Condition: New.

Condition: New. 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. Editor(s): Lodola, Alberto; Stadler, Jeanne. Num Pages: 258 pages, Illustrations. BIC Classification: MMGT. Category: (P) Professional & Vocational. Dimension: 236 x 165 x 19. Weight in Grams: 512. . 2011. 1st Edition. Hardcover. . . . . …

Condition: As New. Unread book in perfect condition.

Condition: New. Brand new! Please provide a physical shipping address.

Condition: As New. Unread book in perfect condition.

Hardcover. Condition: Like New. LIKE NEW. SHIPS FROM MULTIPLE LOCATIONS. book.

Condition: New. 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. Editor(s): Lodola, Alberto; Stadler, Jeanne. Num Pages: 258 pages, Illustrations. BIC Classification: MMGT. Category: (P) Professional & Vocational. Dimension: 236 x 165 x 19. Weight in Grams: 512. . 2011. 1st Edition. Hardcover. . . . . Books ship from the US and Ireland. …

Gebunden. Condition: New. 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 .

Condition: New. Brand New! Fast Delivery This is an International Edition and ship within 24-48 hours. Deliver by FedEx and Dhl, & Aramex, UPS, & USPS and we do accept APO and PO BOX Addresses. Order can be delivered worldwide within 6-10 days and we do have flat rate for up to 2LB. Extra shipping charges will be requested if the Book weight is more than 5 LB. This Item May be shipped from India, United states & United Kingdom. Depending on your location and availability.…

Buch. Condition: Neu. Neuware - This book describes, with references to key source materials,the background to, and conduct of, the principal nonclinical studiesthat 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, andrisk 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.…