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Validation of biopharmaceutical manufacturing processes /
By: American Chemical Society meeting 213th : April 13-17, 1997 : San Francisco, Ca.
Contributor(s): Kelley, Brian D., 1964- | Ramelmeier, R. Andrew | American Chemical Society. Division of Biochemical Technology.
Series: ACS symposium series ; 698.Publisher: Washington, D.C. : American Chemical Society, c1998Description: x, 191 p. : ill. ; 24 cm.Content type: text Media type: unmediated Carrier type: volumeISBN: 9780841235670; 9780841235670 :.Subject(s): Pharmaceutical biotechnology -- CongressesDDC classification: 615.19 Summary: This reference on the validation of biopharmaceutical manufacturing processes describes all aspects of process validation in the licensure of recombinant biologics, for both protein and non-protein products. It covers product synthesis, purification, and filling/finishing.| Item type | Current library | Call number | Copy number | Status | Date due | Barcode | Item holds |
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Standard Loan
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ATU Sligo Yeats Library Main Lending Collection | 615.19 AME (Browse shelf(Opens below)) | 1 | Available | 0051840 |
Total holds: 0
Includes bibliographical references and indexes.
This reference on the validation of biopharmaceutical manufacturing processes describes all aspects of process validation in the licensure of recombinant biologics, for both protein and non-protein products. It covers product synthesis, purification, and filling/finishing.