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Applications of ion chromatography for pharmaceutical and biological products [[electronic resource] /] / edited by Lokesh Bhattacharyya, Jeffrey S. Rohrer
| Applications of ion chromatography for pharmaceutical and biological products [[electronic resource] /] / edited by Lokesh Bhattacharyya, Jeffrey S. Rohrer |
| Pubbl/distr/stampa | Hoboken, N.J., : John Wiley & Sons, Inc., c2012 |
| Descrizione fisica | 1 online resource (477 p.) |
| Disciplina | 660.6/3 |
| Altri autori (Persone) |
BhattacharyyaLokesh
RohrerJeffrey S |
| Soggetto topico |
Ion exchange chromatography
Biological products - Analysis Pharmaceutical industry - Standards |
| ISBN |
1-280-59061-0
9786613620446 1-118-14699-9 1-118-14700-6 |
| Formato | Materiale a stampa  |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
APPLICATIONS OF ION CHROMATOGRAPHY FOR PHARMACEUTICAL AND BIOLOGICAL PRODUCTS; CONTENTS; CONTRIBUTORS; PREFACE; PART I PRINCIPLES, MECHANISM,AND INSTRUMENTATION; 1 ION CHROMATOGRAPHY-PRINCIPLES AND APPLICATIONS; 2 RETENTION PROCESSES IN ION-EXCLUSION CHROMATOGRAPHY: A NEW PERSPECTIVE; 3 PULSED ELECTRO-CHEMICAL DETECTION IN ION CHROMATOGRAPHY; 4 SUPPRESSOR DESIGN AND DETECTION FOR ION CHROMATOGRAPHY; 5 MODELLING AND OPTIMIZATION OF ION CHROMATOGRAPHIC SEPARATIONS OF PHARMACEUTICALLY RELEVANT ORGANIC IONS; PART II PHARMACEUTICAL APPLICATIONS; 6 ION CHROMATOGRAPHY IN PHARMACEUTICAL DRUG ANALYSIS
7 ANALYSIS FOR IMPURITIES BY ION CHROMATOGRAPHY 8 ION CHROMATOGRAPHY ANALYSIS OF AMINOGLYCOSIDE ANTIBIOTICS; 9 USE OF CATION-EXCHANGE ION CHROMATOGRAPHY IN THE ANALYSIS OF PHARMACEUTICALS; 10 COMPREHENSIVE APPROACHES FOR MEASUREMENT OF ACTIVE PHARMACEUTICAL INGREDIENTS, COUNTER-IONS,AND EXCIPIENTS USING HPLC WITH CHARGED AEROSOL DETECTION; 11 HIGH PERFORMANCE ION CHROMATOGRAPHIC ANALYSIS OF CHOLINERGIC COMPOUNDS: CARBACHOLAND BETHANECHOL, AND ASSOCIATED DEGRADATION PRODUCTS; 12 ION CHROMATOGRAPHIC ANALYSIS OF PHARMACEUTICALS FOR AUTHENTICITY AND ADULTERATION 13 ION CHROMATOGRAPHY OF DRUG PRODUCT COUNTER-IONS AND OTHER IONS IN DRUG PRODUCTS 14 SAMPLE PREPARATION TECHNIQUES IN ION CHROMATOGRAPHY FOR PHARMACEUTICAL APPLICATIONS; 15 VALIDATION OF ION CHROMATOGRAPHIC METHODS; 16 PHARMACOPEIAL APPLICATIONS OF ION CHROMATOGRAPHY; PART III BIOTECHNOLOGY APPLICATIONS; 17 GLYCAN ANALYSIS BY HIGH PERFORMANCE ANION EXCHANGE CHROMATOGRAPHY WITH PULSED AMPEROMETRIC DETECTION; 18 MONOSACCHARIDE ANALYSIS OF GLYCOPROTEINS BY HIGH-PERFORMANCE ANION-EXCHANGE CHROMATOGRAPHY WITH PULSED AMPEROMETRIC DETECTION 19 TWO-DIMENSIONAL ION CHROMATOGRAPHY FOR SIMULTANEOUS DETERMINATION OF AMINO ACIDS AND CARBOHYDRATES 20 MONITORING PROTEIN N-GLYCOSYLATION CONSISTENCY USING HPAEC-PAD; 21 OLIGOSACCHARIDE ANALYSIS BY HIGH-PERFORMANCE ANION-EXCHANGE CHROMATOGRAPHY HYPHENATED TO INTEGRATED PULSED AMPEROMETRIC DETECTION AND ON-LINE ION-TRAP MASS SPECTROMETRY; PART IV VACCINE APPLICATIONS; 22 APPLICATIONS OF ION CHROMATOGRAPHY IN BIOLOGICAL PRODUCT ANALYSES 23 HIGH PERFORMANCE ANION-EXCHANGE CHROMATOGRAPHY WITH PULSED AMPEROMETRIC DETECTION (HPAEC-PAD)ANALYSIS OF GBS GLYCOCON JUGATE VACCINES:FROM FERMENTATION TO FINAL PRODUCT 24 STABILITY STUDIES AND CHARACTERIZATION OF MENINGOCOCCAL A, C, Y, AND W135 GLYCOCONJUGATE VACCINE; PART V APPENDICES; Appendix 1 DISSOCIATION CONSTANTS (pKa) OF ORGANICACIDS (AT 20?C); Appendix 2 DISSOCIATION CONSTANTS (pKa) OF COMMON SUGARS AND ALCOHOLS; INDEX |
| Record Nr. | UNINA-9910141309403321 |
| Hoboken, N.J., : John Wiley & Sons, Inc., c2012 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
International IT regulations and compliance [[electronic resource] ] : quality standards in the pharmaceutical and regulated industries / / Siri H. Segalstad
| International IT regulations and compliance [[electronic resource] ] : quality standards in the pharmaceutical and regulated industries / / Siri H. Segalstad |
| Autore | Segalstad Siri H |
| Pubbl/distr/stampa | Chichester, West Sussex, United Kingdom, : Wiley, 2008 |
| Descrizione fisica | 1 online resource (340 p.) |
| Disciplina |
615
615.19 |
| Soggetto topico |
Pharmaceutical technology - Standards
Pharmaceutical industry - Standards Pharmaceutical industry - Quality control Drugs - Standards |
| Soggetto genere / forma | Electronic books. |
| ISBN |
1-282-34277-0
9786612342776 0-470-72182-0 0-470-72183-9 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
International IT Regulations and Compliance; Contents; Preface and Acknowledgements; 1 Quality Standards; 1.1 What Quality Is; 1.2 Mandatory and Voluntary Standards; 1.3 Pharmaceutical Industry Regulations; 1.4 US GxP Regulations; 1.5 European GxP Regulations; 1.6 Other GxP Regulations; 1.7 Good Manufacturing Practice; 1.8 Good Laboratory Practice; 1.9 Good Clinical Practice; 1.10 Medical Device Standards; 1.11 IT Systems in the GxP and Medical Device Regulations; 1.12 GAMP; 1.13 Mandatory Quality Standards in Other Industries; 1.14 Legal Issues; 1.15 The ISO; 1.16 The ASTM; 1.17 The IEEE
1.18 TasksReferences; 2 Regulatory Requirements for IT Systems; 2.1 Introduction; 2.2 US Requirements; 2.3 EU Requirements; 2.4 21 CFR Part 11; 2.5 The 'Part 11 Project'; 2.6 EU GMP Annex 11; 2.7 The PIC Document PI 011 Recommendation on Computerized Systems in Regulated 'GxP' Environments; 2.8 GAMP; 2.9 The ISO 9000 Series; 2.10 A Comparison between the Standards; 2.11 Conclusion; 2.12 Tasks; References; 3 IT Security; 3.1 Introduction; 3.2 Continuous Connections - Wireless Networks; 3.3 Threats; 3.4 The Security Policy; 3.5 Tasks; References; 4 Quality Management Systems 4.1 An Introduction to QMS4.2 Definitions; 4.3 Principles for Quality Management; 4.4 Quality Management System Levels; 4.5 Creating a QMS; 4.6 Roles and Responsibilities; 4.7 Work Processes; 4.8 Controlled Documents; 4.9 The Quality Policy; 4.10 The Quality Manual; 4.11 Standard Operating Procedures; 4.12 The Art of Writing an SOP; 4.13 Tasks; References; 5 IT Integrated in the QMS in the User Organization; 5.1 Introduction; 5.2 How to Integrate IT Systems in the QMS; 5.3 Generic Standard Operating Procedures; 5.4 Procedures for Each System; 5.5 Tasks; References 6 IT Integrated in the Supplier's QMS6.1 Introduction; 6.2 Which Standards Should Be Used?; 6.3 The Quality Management System; 6.4 System Development Models; 6.5 Documents for Software Development; 6.6 The Customer-Supplier Relationship; 6.7 Tasks; References; 7 Organization for an IT System; 7.1 Introduction; 7.2 Roles and Responsibilities for a Live System; 7.3 Groups in the IT System Organization; 7.4 Roles and Responsibilities for an IT Validation Project; 7.5 Outsourcing; 7.6 The Service Level Agreement for Outsourcing; 7.7 Consultants; References 8 The Legal Implications of an IT System8.1 Introduction; 8.2 Pharmaceutical Regulations; 8.3 Financial Systems; 8.4 Patent Systems; 8.5 Human Resources Systems; 8.6 Healthcare Systems; 8.7 Systems for Legal Information; Reference; 9 Advanced Quality Management Systems; 9.1 Introduction; 9.2 The Live QMS is a Good QMS; 9.3 Changes; 9.4 How to Keep the QMS Updated; 9.5 Training and Understanding; 9.6 How to use a QMS Effectively as a Tool in the Organization - Not as a Straightjacket; 9.7 Tasks; References; 10 Audits; 10.1 Introduction; 10.2 The ISO 9000 Series; 10.3 TickIT; 10.4 Why Audit? 10.5 Audit in a Risk-Based Environment |
| Record Nr. | UNINA-9910144386003321 |
Segalstad Siri H
|
||
| Chichester, West Sussex, United Kingdom, : Wiley, 2008 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
International IT regulations and compliance [[electronic resource] ] : quality standards in the pharmaceutical and regulated industries / / Siri H. Segalstad
| International IT regulations and compliance [[electronic resource] ] : quality standards in the pharmaceutical and regulated industries / / Siri H. Segalstad |
| Autore | Segalstad Siri H |
| Pubbl/distr/stampa | Chichester, West Sussex, United Kingdom, : Wiley, 2008 |
| Descrizione fisica | 1 online resource (340 p.) |
| Disciplina |
615
615.19 |
| Soggetto topico |
Pharmaceutical technology - Standards
Pharmaceutical industry - Standards Pharmaceutical industry - Quality control Drugs - Standards |
| ISBN |
1-282-34277-0
9786612342776 0-470-72182-0 0-470-72183-9 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
International IT Regulations and Compliance; Contents; Preface and Acknowledgements; 1 Quality Standards; 1.1 What Quality Is; 1.2 Mandatory and Voluntary Standards; 1.3 Pharmaceutical Industry Regulations; 1.4 US GxP Regulations; 1.5 European GxP Regulations; 1.6 Other GxP Regulations; 1.7 Good Manufacturing Practice; 1.8 Good Laboratory Practice; 1.9 Good Clinical Practice; 1.10 Medical Device Standards; 1.11 IT Systems in the GxP and Medical Device Regulations; 1.12 GAMP; 1.13 Mandatory Quality Standards in Other Industries; 1.14 Legal Issues; 1.15 The ISO; 1.16 The ASTM; 1.17 The IEEE
1.18 TasksReferences; 2 Regulatory Requirements for IT Systems; 2.1 Introduction; 2.2 US Requirements; 2.3 EU Requirements; 2.4 21 CFR Part 11; 2.5 The 'Part 11 Project'; 2.6 EU GMP Annex 11; 2.7 The PIC Document PI 011 Recommendation on Computerized Systems in Regulated 'GxP' Environments; 2.8 GAMP; 2.9 The ISO 9000 Series; 2.10 A Comparison between the Standards; 2.11 Conclusion; 2.12 Tasks; References; 3 IT Security; 3.1 Introduction; 3.2 Continuous Connections - Wireless Networks; 3.3 Threats; 3.4 The Security Policy; 3.5 Tasks; References; 4 Quality Management Systems 4.1 An Introduction to QMS4.2 Definitions; 4.3 Principles for Quality Management; 4.4 Quality Management System Levels; 4.5 Creating a QMS; 4.6 Roles and Responsibilities; 4.7 Work Processes; 4.8 Controlled Documents; 4.9 The Quality Policy; 4.10 The Quality Manual; 4.11 Standard Operating Procedures; 4.12 The Art of Writing an SOP; 4.13 Tasks; References; 5 IT Integrated in the QMS in the User Organization; 5.1 Introduction; 5.2 How to Integrate IT Systems in the QMS; 5.3 Generic Standard Operating Procedures; 5.4 Procedures for Each System; 5.5 Tasks; References 6 IT Integrated in the Supplier's QMS6.1 Introduction; 6.2 Which Standards Should Be Used?; 6.3 The Quality Management System; 6.4 System Development Models; 6.5 Documents for Software Development; 6.6 The Customer-Supplier Relationship; 6.7 Tasks; References; 7 Organization for an IT System; 7.1 Introduction; 7.2 Roles and Responsibilities for a Live System; 7.3 Groups in the IT System Organization; 7.4 Roles and Responsibilities for an IT Validation Project; 7.5 Outsourcing; 7.6 The Service Level Agreement for Outsourcing; 7.7 Consultants; References 8 The Legal Implications of an IT System8.1 Introduction; 8.2 Pharmaceutical Regulations; 8.3 Financial Systems; 8.4 Patent Systems; 8.5 Human Resources Systems; 8.6 Healthcare Systems; 8.7 Systems for Legal Information; Reference; 9 Advanced Quality Management Systems; 9.1 Introduction; 9.2 The Live QMS is a Good QMS; 9.3 Changes; 9.4 How to Keep the QMS Updated; 9.5 Training and Understanding; 9.6 How to use a QMS Effectively as a Tool in the Organization - Not as a Straightjacket; 9.7 Tasks; References; 10 Audits; 10.1 Introduction; 10.2 The ISO 9000 Series; 10.3 TickIT; 10.4 Why Audit? 10.5 Audit in a Risk-Based Environment |
| Record Nr. | UNINA-9910830674403321 |
|
Segalstad Siri H
|
||
| Chichester, West Sussex, United Kingdom, : Wiley, 2008 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
International IT regulations and compliance [[electronic resource] ] : quality standards in the pharmaceutical and regulated industries / / Siri H. Segalstad
| International IT regulations and compliance [[electronic resource] ] : quality standards in the pharmaceutical and regulated industries / / Siri H. Segalstad |
| Autore | Segalstad Siri H |
| Pubbl/distr/stampa | Chichester, West Sussex, United Kingdom, : Wiley, 2008 |
| Descrizione fisica | 1 online resource (340 p.) |
| Disciplina |
615
615.19 |
| Soggetto topico |
Pharmaceutical technology - Standards
Pharmaceutical industry - Standards Pharmaceutical industry - Quality control Drugs - Standards |
| ISBN |
1-282-34277-0
9786612342776 0-470-72182-0 0-470-72183-9 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
International IT Regulations and Compliance; Contents; Preface and Acknowledgements; 1 Quality Standards; 1.1 What Quality Is; 1.2 Mandatory and Voluntary Standards; 1.3 Pharmaceutical Industry Regulations; 1.4 US GxP Regulations; 1.5 European GxP Regulations; 1.6 Other GxP Regulations; 1.7 Good Manufacturing Practice; 1.8 Good Laboratory Practice; 1.9 Good Clinical Practice; 1.10 Medical Device Standards; 1.11 IT Systems in the GxP and Medical Device Regulations; 1.12 GAMP; 1.13 Mandatory Quality Standards in Other Industries; 1.14 Legal Issues; 1.15 The ISO; 1.16 The ASTM; 1.17 The IEEE
1.18 TasksReferences; 2 Regulatory Requirements for IT Systems; 2.1 Introduction; 2.2 US Requirements; 2.3 EU Requirements; 2.4 21 CFR Part 11; 2.5 The 'Part 11 Project'; 2.6 EU GMP Annex 11; 2.7 The PIC Document PI 011 Recommendation on Computerized Systems in Regulated 'GxP' Environments; 2.8 GAMP; 2.9 The ISO 9000 Series; 2.10 A Comparison between the Standards; 2.11 Conclusion; 2.12 Tasks; References; 3 IT Security; 3.1 Introduction; 3.2 Continuous Connections - Wireless Networks; 3.3 Threats; 3.4 The Security Policy; 3.5 Tasks; References; 4 Quality Management Systems 4.1 An Introduction to QMS4.2 Definitions; 4.3 Principles for Quality Management; 4.4 Quality Management System Levels; 4.5 Creating a QMS; 4.6 Roles and Responsibilities; 4.7 Work Processes; 4.8 Controlled Documents; 4.9 The Quality Policy; 4.10 The Quality Manual; 4.11 Standard Operating Procedures; 4.12 The Art of Writing an SOP; 4.13 Tasks; References; 5 IT Integrated in the QMS in the User Organization; 5.1 Introduction; 5.2 How to Integrate IT Systems in the QMS; 5.3 Generic Standard Operating Procedures; 5.4 Procedures for Each System; 5.5 Tasks; References 6 IT Integrated in the Supplier's QMS6.1 Introduction; 6.2 Which Standards Should Be Used?; 6.3 The Quality Management System; 6.4 System Development Models; 6.5 Documents for Software Development; 6.6 The Customer-Supplier Relationship; 6.7 Tasks; References; 7 Organization for an IT System; 7.1 Introduction; 7.2 Roles and Responsibilities for a Live System; 7.3 Groups in the IT System Organization; 7.4 Roles and Responsibilities for an IT Validation Project; 7.5 Outsourcing; 7.6 The Service Level Agreement for Outsourcing; 7.7 Consultants; References 8 The Legal Implications of an IT System8.1 Introduction; 8.2 Pharmaceutical Regulations; 8.3 Financial Systems; 8.4 Patent Systems; 8.5 Human Resources Systems; 8.6 Healthcare Systems; 8.7 Systems for Legal Information; Reference; 9 Advanced Quality Management Systems; 9.1 Introduction; 9.2 The Live QMS is a Good QMS; 9.3 Changes; 9.4 How to Keep the QMS Updated; 9.5 Training and Understanding; 9.6 How to use a QMS Effectively as a Tool in the Organization - Not as a Straightjacket; 9.7 Tasks; References; 10 Audits; 10.1 Introduction; 10.2 The ISO 9000 Series; 10.3 TickIT; 10.4 Why Audit? 10.5 Audit in a Risk-Based Environment |
| Record Nr. | UNINA-9910840974703321 |
|
Segalstad Siri H
|
||
| Chichester, West Sussex, United Kingdom, : Wiley, 2008 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Pharmazeutische Produkte und Verfahren [[electronic resource] /] / hrsg. von Gerd Kutz und Armin Wolff
| Pharmazeutische Produkte und Verfahren [[electronic resource] /] / hrsg. von Gerd Kutz und Armin Wolff |
| Pubbl/distr/stampa | Weinheim, : Wiley-VCH, 2007 |
| Descrizione fisica | 1 online resource (467 p.) |
| Disciplina |
614.35
615.19 |
| Altri autori (Persone) |
KutzGerd
WolffArmin |
| Soggetto topico |
Pharmaceutical technology
Pharmaceutical industry - Standards |
| Soggetto genere / forma | Electronic books. |
| ISBN |
3-527-66021-6
1-280-92177-3 9786610921775 3-527-61113-4 3-527-61114-2 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | ger |
| Nota di contenuto | Pharmazeutische Produkte und Verfahren; Inhaltsverzeichnis; Autorenverzeichnis; 1 Einführung; 2 Arzneiformen, Arzneimittel, Good Manufacturing Practices und Qualität; 3 Anforderungen an Produktionsanlagen und deren Betrieb; 4 Pharmazeutische Produktionsprozesse für ausgewählte Arzneiformen; Glossar; Sachregister |
| Record Nr. | UNINA-9910144335003321 |
| Weinheim, : Wiley-VCH, 2007 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Pharmazeutische Produkte und Verfahren [[electronic resource] /] / hrsg. von Gerd Kutz und Armin Wolff
| Pharmazeutische Produkte und Verfahren [[electronic resource] /] / hrsg. von Gerd Kutz und Armin Wolff |
| Pubbl/distr/stampa | Weinheim, : Wiley-VCH, 2007 |
| Descrizione fisica | 1 online resource (467 p.) |
| Disciplina |
614.35
615.19 |
| Altri autori (Persone) |
KutzGerd
WolffArmin |
| Soggetto topico |
Pharmaceutical technology
Pharmaceutical industry - Standards |
| ISBN |
3-527-66021-6
1-280-92177-3 9786610921775 3-527-61113-4 3-527-61114-2 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | ger |
| Nota di contenuto | Pharmazeutische Produkte und Verfahren; Inhaltsverzeichnis; Autorenverzeichnis; 1 Einführung; 2 Arzneiformen, Arzneimittel, Good Manufacturing Practices und Qualität; 3 Anforderungen an Produktionsanlagen und deren Betrieb; 4 Pharmazeutische Produktionsprozesse für ausgewählte Arzneiformen; Glossar; Sachregister |
| Record Nr. | UNINA-9910830152103321 |
| Weinheim, : Wiley-VCH, 2007 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Pharmazeutische Produkte und Verfahren [[electronic resource] /] / hrsg. von Gerd Kutz und Armin Wolff
| Pharmazeutische Produkte und Verfahren [[electronic resource] /] / hrsg. von Gerd Kutz und Armin Wolff |
| Pubbl/distr/stampa | Weinheim, : Wiley-VCH, 2007 |
| Descrizione fisica | 1 online resource (467 p.) |
| Disciplina |
614.35
615.19 |
| Altri autori (Persone) |
KutzGerd
WolffArmin |
| Soggetto topico |
Pharmaceutical technology
Pharmaceutical industry - Standards |
| ISBN |
3-527-66021-6
1-280-92177-3 9786610921775 3-527-61113-4 3-527-61114-2 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | ger |
| Nota di contenuto | Pharmazeutische Produkte und Verfahren; Inhaltsverzeichnis; Autorenverzeichnis; 1 Einführung; 2 Arzneiformen, Arzneimittel, Good Manufacturing Practices und Qualität; 3 Anforderungen an Produktionsanlagen und deren Betrieb; 4 Pharmazeutische Produktionsprozesse für ausgewählte Arzneiformen; Glossar; Sachregister |
| Record Nr. | UNINA-9910841606503321 |
| Weinheim, : Wiley-VCH, 2007 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
日本PDA学術誌 GMPとバリデーション [[ニホンPDAガクジュツシGMPトバリデーション]]
| 日本PDA学術誌 GMPとバリデーション [[ニホンPDAガクジュツシGMPトバリデーション]] |
| Pubbl/distr/stampa | Tōkyō, : Nihon PDA, ©1999- |
| Descrizione fisica | 1 online resource |
| Soggetto topico |
Pharmaceutical industry - Standards - Japan
Pharmaceutical technology - Standards - Japan Drugs - Standards - Japan Pharmaceutical Preparations - standards Drug Industry - standards Quality Control Technology, Pharmaceutical - standards Drugs - Standards Pharmaceutical industry - Standards Pharmaceutical technology - Standards |
| Soggetto genere / forma | Periodicals. |
| ISSN | 1881-1728 |
| Formato | Materiale a stampa |
| Livello bibliografico | Periodico |
| Lingua di pubblicazione | jpn |
| Altri titoli varianti |
PDA JOURNAL OF GMP AND VALIDATION IN JAPAN
NIHON PDA GAKUJYUTSUSHI GMP TO BARIDESHON Nihon PDA gakujutsushi GMP to baridēshon |
| Record Nr. | UNISA-996199837103316 |
| Tōkyō, : Nihon PDA, ©1999- | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. di Salerno | ||
| ||
日本PDA学術誌 GMPとバリデーション [[ニホンPDAガクジュツシGMPトバリデーション]]
| 日本PDA学術誌 GMPとバリデーション [[ニホンPDAガクジュツシGMPトバリデーション]] |
| Pubbl/distr/stampa | Tōkyō, : Nihon PDA, ©1999- |
| Descrizione fisica | 1 online resource |
| Soggetto topico |
Pharmaceutical industry - Standards - Japan
Pharmaceutical technology - Standards - Japan Drugs - Standards - Japan Pharmaceutical Preparations - standards Drug Industry - standards Quality Control Technology, Pharmaceutical - standards Drugs - Standards Pharmaceutical industry - Standards Pharmaceutical technology - Standards |
| Soggetto genere / forma | Periodicals. |
| ISSN | 1881-1728 |
| Formato | Materiale a stampa |
| Livello bibliografico | Periodico |
| Lingua di pubblicazione | jpn |
| Altri titoli varianti |
PDA JOURNAL OF GMP AND VALIDATION IN JAPAN
NIHON PDA GAKUJYUTSUSHI GMP TO BARIDESHON Nihon PDA gakujutsushi GMP to baridēshon |
| Record Nr. | UNINA-9910143541103321 |
| Tōkyō, : Nihon PDA, ©1999- | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
