1.

Record Nr.

UNINA9910780897403321

Titolo

Twenty-five years of constructive type theory [[electronic resource] ] : proceedings of a congress held in Venice, October 1995 / / edited by Giovanni Sambin and Jan M. Smith

Pubbl/distr/stampa

Oxford, : Clarendon Press

New York, : Oxford University Press, 1998

ISBN

0-19-191654-4

1-280-81972-3

9786610819720

0-19-158903-9

Descrizione fisica

1 online resource (292 p.)

Collana

Oxford logic guides ; ; 36

Oxford science publications

Altri autori (Persone)

SambinGiovanni

SmithJan M

Disciplina

511.3

Soggetti

Type theory

Logic, Symbolic and mathematical

Lingua di pubblicazione

Inglese

Formato

Materiale a stampa

Livello bibliografico

Monografia

Note generali

Previously issued in print: Oxford: Clarendon Press, 1998.

Nota di bibliografia

Includes bibliographical references.

Nota di contenuto

Cover; Contents; 1. Yet another constructivization of classical logic; 2. Extension of Martin-Löf's type theory with record types and subtyping; 3. Type-theoretical checking and philosophy of mathematics; 4. The Hahn-Banach theorem in type theory; 5. A realizability interpretation of Martin-Löf's type theory; 6. The groupoid interpretation of type theory; 7. Analytic program derivation in type theory; 8. An intuitionistic theory of types; 9. On storage operators; 10. On universes in type theory; 11. How to believe a machine-checked proof

12. Building up a toolbox for Martin-Löf's type theory: subset theory13. An introduction to well-ordering proofs in Martin-Löf's type theory; 14. Variable-free formalization of the Curry-Howard theory; 15. The forget-restore principle: a paradigmatic example

Sommario/riassunto

Martin-Löf type theory is an important and practical formalisation of the foundations of mathematics. This volume celebrates the 25th anniversary of the birth of the subject, and is a record of areas of



activity and of its early development.

2.

Record Nr.

UNINA9910782037503321

Autore

Wessner Charles W

Titolo

Partnering against terrorism [[electronic resource] ] : summary of a workshop / / Charles W. Wessner

Pubbl/distr/stampa

Washington, D.C., : National Academy Press, c2005

ISBN

0-309-16512-1

1-280-74206-2

9786610742066

0-309-54616-8

Descrizione fisica

1 online resource (163 p.)

Collana

Government-industry partnerships

Disciplina

363.325/15250973

Soggetti

Terrorism - United States - Prevention

Public-private sector cooperation - United States

Technology and state - United States

Lingua di pubblicazione

Inglese

Formato

Materiale a stampa

Livello bibliografico

Monografia

Note generali

Sponsored by Committee on Government-Industry Partnerships for the Development of New Technologies, Board on Science, Technology, and Economic Policy, Policy and Global Affairs, National Research Council of the National Academies.

Nota di bibliografia

Includes bibliographical references (p. 138-145).

Nota di contenuto

""Front Matter""; ""Contents""; ""I. INTRODUCTION""; ""II. PROCEEDINGS""; ""Welcome""; ""Introduction""; ""Panel I: Partnering to Meet the New Security Challenge""; ""Panel II: Best Practice Examples of Public-Private Partnerships""; ""Panel III: Partnerships Against Bioterrorism""; ""Panel IV: Partnering for National Security""; ""Panel V: Roundtable on Partnering for National Missions: Defense, Health and Energy""; ""Closing Remarks""; ""III. APPENDIXES""; ""A. Biographies of Speakers""; ""B. Participants List""; ""C. Bibliography""



3.

Record Nr.

UNINA9910955154003321

Titolo

Pharmaceutical manufacturing handbook : regulations and quality / / [edited by] Shayne Cox Gad

Pubbl/distr/stampa

Hoboken, N.J., : Wiley-Interscience, c2008

ISBN

9786611237523

9781281237521

1281237523

9780470259832

0470259833

9780470259825

0470259825

Edizione

[1st ed.]

Descrizione fisica

1 online resource (857 pages)

Collana

Pharmaceutical Development Series

Altri autori (Persone)

GadShayne C. <1948->

Disciplina

615.19

615/.19

Soggetti

Pharmaceutical technology - Quality control

Pharmacy - Law and legislation - United States

Lingua di pubblicazione

Inglese

Formato

Materiale a stampa

Livello bibliografico

Monografia

Nota di bibliografia

Includes bibliographical references and index.

Nota di contenuto

PHARMACEUTICAL MANUFACTURING HANDBOOK Regulations and Quality; CONTRIBUTORS; CONTENTS; PREFACE; SECTION 1 GOOD MANUFACTURING PRACTICES (GMP) AND OTHER FDA GUIDELINES; 1.1 Good Manufacturing Practices (GMPs) and Related FDA Guidelines; 1.2 Enforcement of Current Good Manufacturing Practices; 1.3 Scale-Up and Postapproval Changes (SUPAC) Regulations; 1.4 GMP-Compliant Propagation of Human Multipotent Mesenchymal Stromal Cells; SECTION 2 INTERNATIONAL REGULATIONS OF GOOD MANUFACTURING PRACTICES

2.1 National GMP Regulations and Codes and International GMP Guides and Guildelines: Correspondences and Differences; SECTION 3 QUALITY; 3.1 Analytical and Computational Methods and Examples for Designing and Controlling Total Quality Management Pharmaceutical Manufacturing Systems; 3.2 Role of Quality Systems and Audits in Phatmaceutical Manufacturing Environment; 3.3 Creating and Managing



a Quality Management System; 3.4 Quality Process Improvement; SECTION 4 PROCESS ANALYTICAL TECHNOLOGY (PAT); 4.1 Case for Process Analytical Technology: Regulatory and Industrial Perspectives

4.2 Process Analytical Technology; 4.3 Chemical Imaging and Chemometrics: Useful Tools for Process Analytical Technology; SECTION 5 PERSONNEL; 5.1 Personnel Training in Pharmaceutical Manufacturing; SECTION 6 CONTAMINATION AND CONTAMINATION CONTROL; 6.1 Origin of Contamination; 6.2 Quantitation of Markers for Gram-Negative and Gram-Positive Endotoxins in Work Environment and as Contaminants in Pharmaceutical Products Using Gas Chromatography-Tandem Mass Spectrometry; 6.3 Microbiology of Nonsterile Pharmaceutical Manufacturing; SECTION 7 DRUG STABILITY

7.1 Stability and Shelf Life of Pharmaceutical Products; 7.2 Drug Stability; 7.3 Effect of Packaging on Stability of Drugs and Drug Products; 7.4 Pharmaceutical Product Stability; 7.5 Alternative Accelerated Methods for Studying Drug Stability: Variable-Parameter Kinetics; SECTION 8 VALIDATION; 8.1 Analytical Method Validation: Principles and Practices; 8.2 Analytical Method Validation and Quality Assurance; 8.3 Validation of Laboratory Instruments; 8.4 Pharmaceutical Manufacturing Validation Principles; INDEX

Sommario/riassunto

With its coverage of Food and Drug Administration regulations, international regulations, good manufacturing practices, and process analytical technology, this handbook offers complete coverage of the regulations and quality control issues that govern pharmaceutical manufacturing. In addition, the book discusses quality assurance and validation, drug stability, and contamination control, all key aspects of pharmaceutical manufacturing that are heavily influenced by regulatory guidelines.