Aami (7 results)

paperback. 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.

Paperback. 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.

Condition: Good. Pages intact with minimal writing/highlighting. The binding may be loose and creased. Dust jackets/supplements are not included. Stock photo provided. Product includes identifying sticker. Better World Books: Buy Books. Do Good.

Condition: Very Good. Former library copy. Pages intact with possible writing/highlighting. Binding strong with minor wear. Dust jackets/supplements may not be included. Includes library markings. Stock photo provided. Product includes identifying sticker. Better World Books: Buy Books. Do Good.

Condition: Good. Good; Softcover; Moderate wear to the covers; Unblemished textblock edges; Underlining to about 10 pages, otherwise the endpapers and all text pages are clean and unmarked; Good binding; This book will be shipped in a sturdy cardboard box with foam padding; Large Format (Quatro, 10.75" - 11.75" tall); Light green covers with title in black lettering; 1998, AAMI Publishing; 100 pages; "The Quality System Compendium: Gmp Requirements & Industry Practice," by AAMI Publishing. …

Soft cover. Condition: New. 4th Edition. *NEW* CGMP Requirements and Industry Practice The fourth edition, provides a timely and comprehensive view of the rapidly evolving world of international medical device regulations. Since the 2015 publication of the third edition of this Compendium, the medical device regulatory landscape has undergone fundamental changes that impact many aspects of the global medical device community. This updated Compendium builds on the success of the third edition with new and expanded information directly relevant to today s international medical device environment, including very readable and directly applicable material on such important topics as the Food and Drug Administration (FDA) 21 CFR Part 820 and ISO 13485:2016, the Medical Device Single Audit Program (MDSAP), the EU Medical Device Regulation, the EU In Vitro Diagnostic Regulation, and evolving standards for software validation and risk management.…

Paperback. Condition: Fine. Third Edition of 2015. A sharp unused copy.