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Pharmaceutical dosage forms : parenteral medications / edited by Kenneth E. Avis, Herbert A. Lieberman, Leon Lachman.

Contributor(s): Avis, Kenneth E, 1918- | Lieberman, Herbert A, 1920- | Lachman, Leon, 1929-.
Material type: TextTextPublisher: New York ; New Delhi : M. Dekker, c1993Edition: 2nd ed., rev. and expanded.Description: 3 v. : ill. ; 26 cm.ISBN: 0824785762 (v. 1 : alk. paper); 9780824785765; 0824787714 (v. 2 : alk. paper); 9780824787714; 0824790200 (v. 3 : alk. paper); 9780824790202.Subject(s): Parenteral solutions | Pharmaceutical technology | Infusions, Parenteral | Technology, PharmaceuticalDDC classification: 615.19 Online resources: Publisher description | WorldCat details
Contents:
Table of contents Volume 1: -- 1. The parenteral dosage form and its historical development -- 2. Parenteral drug administration: Routes, precautions, problems, complications, and drug delivery systems -- 3. Biopharmaceutics of injectable medications -- 4. Preformulation research of parenteral medications -- 5. Formulation of small volume parenterals -- 6. Formulation of large volume parenterals -- 7. Parenteral products of peptides and proteins -- 8. Sterile diagnostics -- 9. Glass containers for parenterals -- 10. Use of plastics for parenteral packaging -- 11. Elastomeric closures for parenterals -- 12. Parenteral products in hospital and home care -- Volume 2: -- 1. The processing of small volume parenterals and related sterile products -- 2. Factors involved in manufacturing large volume parenterals -- 3. Freeze drying: Principles and practice -- 4. Design considerations for a parenteral production facility -- 5. Biopharmaceutical manufacturing facility design -- 6. Personnel: The key factor in clean room operations -- 7. Environmental control in parenteral drug manufacturing -- 8. Industrial sterilization: A review of current principles and practices -- 9. Development of ophthalmic formulations -- Volume 3: -- 1. Quality assurance -- 2. Records and reports -- 3. Particulate matter -- 4. Validation of sterilization processes and sterile products -- 5. Federal regulation of parenterals -- 6. Systematic audits of parenteral drug good manufacturing practices -- 7. Medical devices: Design, manufacture, and quality control -- 8. Quality assurance for medical devices -- 9. Regulatory and GMP considerations for medical devices.
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Item type Current location Collection Call number Copy number Status Date due Barcode Item holds
Text Text EWU Library
Reserve Section
Non-fiction 615.19 PHA 2005 (Browse shelf) C-1 Not For Loan 16084
Text Text EWU Library
Reserve Section
Non-fiction 615.19 PHA 2005 (Browse shelf) C-1 Not For Loan 16085
Text Text EWU Library
Reserve Section
Non-fiction 615.19 PHA 2005 (Browse shelf) C-1 Not For Loan 16086
Text Text EWU Library
Reserve Section
Non-fiction 615.19 PHA 2005 (Browse shelf) C-2 Not For Loan 21150
Text Text EWU Library
Reserve Section
Non-fiction 615.19 PHA 2005 (Browse shelf) C-2 Not For Loan 21151
Text Text EWU Library
Reserve Section
Non-fiction 615.19 PHA 2005 (Browse shelf) C-2 Not For Loan 21152
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Includes bibliographical references and index.

Table of contents Volume 1: --
1. The parenteral dosage form and its historical development --
2. Parenteral drug administration: Routes, precautions, problems, complications, and drug delivery systems --
3. Biopharmaceutics of injectable medications --
4. Preformulation research of parenteral medications --
5. Formulation of small volume parenterals --
6. Formulation of large volume parenterals --
7. Parenteral products of peptides and proteins --
8. Sterile diagnostics --
9. Glass containers for parenterals --
10. Use of plastics for parenteral packaging --
11. Elastomeric closures for parenterals --
12. Parenteral products in hospital and home care --
Volume 2: --
1. The processing of small volume parenterals and related sterile products --
2. Factors involved in manufacturing large volume parenterals --
3. Freeze drying: Principles and practice --
4. Design considerations for a parenteral production facility --
5. Biopharmaceutical manufacturing facility design --
6. Personnel: The key factor in clean room operations --
7. Environmental control in parenteral drug manufacturing --
8. Industrial sterilization: A review of current principles and practices --
9. Development of ophthalmic formulations --
Volume 3: --
1. Quality assurance --
2. Records and reports --
3. Particulate matter --
4. Validation of sterilization processes and sterile products --
5. Federal regulation of parenterals --
6. Systematic audits of parenteral drug good manufacturing practices --
7. Medical devices: Design, manufacture, and quality control --
8. Quality assurance for medical devices --
9. Regulatory and GMP considerations for medical devices.

Pharmacy

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