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The quality control of medicines : proceedings of the 35th International Congress of Pharmaceutical Sciences, Dublin 1975 /
The Quality Control of Medicines documents the proceedings of the 35th International Congress of Pharmaceutical Sciences, organized by the Pharmaceutical Society of Ireland on behalf of the Federation Internationale Pharmaceutique, held in Dublin, on 1-5 September 1975. The theme chosen for the Cong...
| Clasificación: | Libro Electrónico |
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| Autor Corporativo: | |
| Otros Autores: | , |
| Formato: | Electrónico Congresos, conferencias eBook |
| Idioma: | Inglés |
| Publicado: |
Amsterdam ; New York :
Elsevier,
1976.
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| Temas: | |
| Acceso en línea: | Texto completo |
Tabla de Contenidos:
- Front Cover; The Quality Control of Medicines; Copyright Page; Introduction; List of contributors; Table of Contents; Inaugural address; The quality control of medicines: A national and international responsibility; Part I: Main symposium. The basis for the quality control of medicines; Chapter 1. Chemical And Physical Aspects Of The Control Of Medicines; RESEARCH AND DEVELOPMENT; PHARMACEUTICAL PREPARATIONS; AUTOMATION; CONCLUSION; SUMMARY; Chapter 2. Biological Aspects Of The Control Of Medicines; ANTIGEN ANTIBODY REACTION; REFERENCES.
- Chapter 3. New concepts and standards of quality control as applied to controlled drug delivery systemsINTRODUCTION; QUALITY STANDARDS AND CONTROL METHODS FOR POLYMERIC MATERIALS; STANDARDS AND CONTROL METHODS IN DELIVERY SYSTEM MANUFACTURING OPERATIONS; STERILIZATION METHODS AND STERILITY STANDARDS; ""FUNCTIONALITY"": CONTROL METHODS AND STANDARDS; CONCLUSIONS; SUMMARY; Chapter 4. Storage problems associated with the control of medicines; SUPERVISION AND PROLONGATION OF STORABILITY; REFERENCES; Chapter 5. International problems in the control of medicines; Part II: Parallel symposia.
- Section 1: Physicochemical analysisChapter6. Spectral methods and in particular spectrofluorimetry; RECALL OF THE FUNDAMENTAL PRINCIPLES; INTRODUCTION TO THE EXPERIMENTAL METHOD; CHARACTERISTICS OF FLUORESCENT MOLECULES; ANALYTICAL APPLICATIONS; COMPARISON OF FLUORESCENCE WITH OTHER SPECTRAL METHODS; ENVIRONMENTAL EFFECTS AND LIMITATIONS; CONCLUSIONS; ACKNOWLEDGEMENTS; REFERENCES; Chapter7. The uses of mass spectrometry in the quality control of drugs; INTRODUCTION; DETECTION LIMIT, IDENTIFICATION LIMIT AND SAMPLE AMOUNTS. DERIVATISATION-REACTIONS; USES IN THE QUALITY CONTROL OF DRUGS.
- PROCEDURE FOR MASS SPECTROMETRIC IONISATIONCOMBINATIONS OF MASS SPECTROMETRY WITH CHROMATOGRAPHIC SEPARATION PROCEDURES; REFERENCES; Chapter8. Microwave discharge and afterglow excited emission spectra fordetection in gas chromatography; THE MICROWAVE GAS DISCHARGE; AFTERGLOW EXCITED MOLECULAR EMISSION SPECTRA; REFERENCES; Chapter9. Automation in pharmaceutical analysis; DATA PROCESSING IN THE ADMINISTRATIVE ASPECT OF PHARMACEUTICAL QUALITY CONTROL; DATA PROCESSING IN THE LABORATORY; AUTOMATIC ANALYSERS; PREFERRED RANGES FOR THE USE OF AUTOMATIC ANALYSERS; CONCLUDING REMARKS; REFERENCES.
- Section 2: Microbiological aspectsChapter10. Testing procedures for sterile products; INTRODUCTION; CONCLUSIONS; REFERENCES; Chapter11. Microbiological aspects in the control of non-sterile products; INTRODUCTION; MICROBIOLOGICAL PURITY-STANDARDS OF NON-STERILE PRODUCT; PRODUCT; MICROBIOLOGICAL ASPECTS IN THE DEVELOPMENT OF A PRODUCT; QUALITY ASSURANCE SYSTEM; REFERENCES; Chapter12. Preservation and sterility of ophthalmic preparations and devices; STERILITY REQUIREMENTS FOR OPHTHALMIC PREPARATIONS; WHEN AND WHY IS PRESERVATION REQUIRED?; THE FINAL CONTAINER; REFERENCES.