Lieberman, H. A <br/><br/>
Pharmaceutical dosage forms/ 
H. A Lieberman 
 - 2nd ed. 
 - New York:  Marcel Dekker,  2005. 
<br/><br/>Chapter 1 Quality Assurance / Samir A. Hanna --<br/>chapter 2 Records and Reports / David C. Fry Karl L. Hofmann --<br/>chapter 3 Particulate Matter / Patrick P. DeLuca Julius Z. Knapp --<br/>chapter 4 Validation of Sterilization Processes and Sterile Products / James Agalloco James Akers --<br/>chapter 5 Federal Regulation of Parenterals / Terry E. Munson Jonas L. Bassen Bernard T. Loftus --<br/>chapter 6 Systematic Audits of Parenteral Drug Good Manufacturing Practices / Ronald F. Tetzlaff --<br/>chapter 7 Medical Devices: Design, Manufacture, and Quality Control / David H. Wayt --<br/>chapter 8 Quality Assurance for Medical Devices / Carl W. Bruch --<br/>chapter 9 Regulatory and GMP Considerations for Medical Devices / Larry R. Pilot. 
<br/><br/><label>Subjects--Topical Terms: </label><br/> Parenteral solutions<br/>Pharmaceutical technology.
<br/><br/><label>Dewey Class. No.: </label>615.191  / LIE/P