Handbook of pharmaceutical manufacturing formulations. (Record no. 89361)
[ view plain ]
| 000 -LEADER | |
|---|---|
| fixed length control field | 02593cam a22004571i 4500 |
| 001 - CONTROL NUMBER | |
| control field | 9781315102948 |
| 003 - CONTROL NUMBER IDENTIFIER | |
| control field | FlBoTFG |
| 005 - DATE AND TIME OF LATEST TRANSACTION | |
| control field | 20260210180721.0 |
| 006 - FIXED-LENGTH DATA ELEMENTS--ADDITIONAL MATERIAL CHARACTERISTICS--GENERAL INFORMATION | |
| fixed length control field | m d |
| 007 - PHYSICAL DESCRIPTION FIXED FIELD--GENERAL INFORMATION | |
| fixed length control field | cr ||||||||||| |
| 008 - FIXED-LENGTH DATA ELEMENTS--GENERAL INFORMATION | |
| fixed length control field | 191119s2019 flu o 000 0 eng d |
| 040 ## - CATALOGING SOURCE | |
| Original cataloging agency | OCoLC-P |
| Language of cataloging | eng |
| Description conventions | rda |
| -- | pn |
| Transcribing agency | OCoLC-P |
| 020 ## - INTERNATIONAL STANDARD BOOK NUMBER | |
| International Standard Book Number | 9781315102948 |
| Qualifying information | (electronic bk.) |
| 020 ## - INTERNATIONAL STANDARD BOOK NUMBER | |
| International Standard Book Number | 1315102943 |
| Qualifying information | (electronic bk.) |
| 020 ## - INTERNATIONAL STANDARD BOOK NUMBER | |
| International Standard Book Number | 9781351593595 |
| Qualifying information | (ePub ebook) : |
| 020 ## - INTERNATIONAL STANDARD BOOK NUMBER | |
| International Standard Book Number | 1351593595 |
| Qualifying information | (ePub ebook) : |
| 020 ## - INTERNATIONAL STANDARD BOOK NUMBER | |
| Cancelled/invalid ISBN | 9781138103160 (hbk.) |
| 020 ## - INTERNATIONAL STANDARD BOOK NUMBER | |
| International Standard Book Number | 9781351593601 |
| Qualifying information | (PDF ebook) : |
| 020 ## - INTERNATIONAL STANDARD BOOK NUMBER | |
| International Standard Book Number | 1351593609 |
| Qualifying information | (PDF ebook) : |
| 020 ## - INTERNATIONAL STANDARD BOOK NUMBER | |
| International Standard Book Number | 9781351593588 |
| Qualifying information | (electronic bk. : Mobipocket) |
| 020 ## - INTERNATIONAL STANDARD BOOK NUMBER | |
| International Standard Book Number | 1351593587 |
| Qualifying information | (electronic bk. : Mobipocket) |
| 024 7# - OTHER STANDARD IDENTIFIER | |
| Standard number or code | 10.1201/9781315102948 |
| Source of number or code | doi |
| 035 ## - SYSTEM CONTROL NUMBER | |
| System control number | (OCoLC)1129692351 |
| 035 ## - SYSTEM CONTROL NUMBER | |
| System control number | (OCoLC-P)1129692351 |
| 050 #4 - LIBRARY OF CONGRESS CALL NUMBER | |
| Classification number | RS200 |
| 082 04 - DEWEY DECIMAL CLASSIFICATION NUMBER | |
| Classification number | 615.19 |
| Edition number | 23 |
| 100 1# - MAIN ENTRY--PERSONAL NAME | |
| Personal name | Niazi, Sarfaraz, |
| Dates associated with a name | 1949- |
| Relator term | author. |
| 245 10 - TITLE STATEMENT | |
| Title | Handbook of pharmaceutical manufacturing formulations. |
| Number of part/section of a work | Volume two, |
| Name of part/section of a work | Uncompressed solid products / |
| Statement of responsibility, etc | Sarfaraz K. Niazi. |
| 250 ## - EDITION STATEMENT | |
| Edition statement | Third edition. |
| 264 #1 - | |
| -- | Boca Raton : |
| -- | CRC Press, |
| -- | 2019. |
| 300 ## - PHYSICAL DESCRIPTION | |
| Extent | 1 online resource |
| 336 ## - | |
| -- | text |
| -- | rdacontent |
| 337 ## - | |
| -- | computer |
| -- | rdamedia |
| 338 ## - | |
| -- | online resource |
| -- | rdacarrier |
| 500 ## - GENERAL NOTE | |
| General note | Previous edition: New York: Informa Healthcare, 2009. |
| 500 ## - GENERAL NOTE | |
| General note | <P><STRONG>Part I. Regulatory and Manufacturing Guidelines</STRONG></P><P>Chapter 1. U.S. FDA Good Manufacturing Practices</P><P>Chapter 2. Guideline on the Common Technical Document for the Registration of Pharmaceuticals for Human Use</P><P>Chapter 3. Process Validation: General Principles and Practices</P><P>Chapter 4. Bioequivalence Regulatory Compliance</P><P>Chapter 5. Bioequivalence Regulatory Review Process and Audit</P><P>Chapter 6. EU Guidelines to Good Manufacturing Practice: Active Drug Substance</P><P>Chapter 7. FDA Pre-approval Inspections</P><P>Chapter 8. Formulation Factors in Uncompressed Dosage Forms</P><P>Chapter 9: Solid-State Properties.</P><P>Chapter 10: Formulation of Flavor.</P><P><STRONG>Part II. Manufacturing Formulations</STRONG></P><P>Uncompressed Solids Formulations</P><P><STRONG>Part III. Commercial Pharmaceutical Formulations.</STRONG></P><P>Commercial Pharmaceutical Formulations.</P> |
| 588 ## - | |
| -- | OCLC-licensed vendor bibliographic record. |
| 650 #0 - SUBJECT ADDED ENTRY--TOPICAL TERM | |
| Topical term or geographic name as entry element | Drugs |
| General subdivision | Dosage forms. |
| 856 40 - ELECTRONIC LOCATION AND ACCESS | |
| Materials specified | Taylor & Francis |
| Uniform Resource Identifier | <a href="https://www.taylorfrancis.com/books/9781315102948">https://www.taylorfrancis.com/books/9781315102948</a> |
| 856 42 - ELECTRONIC LOCATION AND ACCESS | |
| Materials specified | OCLC metadata license agreement |
| Uniform Resource Identifier | <a href="http://www.oclc.org/content/dam/oclc/forms/terms/vbrl-201703.pdf">http://www.oclc.org/content/dam/oclc/forms/terms/vbrl-201703.pdf</a> |
No items available.