Mirza shahed (54 risultati)

Condizione: New.

Condizione: New.

Paperback. Condizione: New.

Condizione: New. In English.

Condizione: New.

Condizione: New. pp. 124.

Paperback. Condizione: Brand New. 128 pages. 8.66x5.91x0.29 inches. In Stock.

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Taschenbuch. Condizione: Neu. Stress Degradation Studies and Stability-Indicating Analytical Methods | Stress Degradation Studies, Stability-Indicating Assay Methods, HPLC, HPTLC Analysis, Impurities | Mirza Shahed Baig (u. a.) | Taschenbuch | 428 S. | Englisch | 2018 | LAP LAMBERT Academic Publishing | EAN 9786139917419 | Verantwortliche Person für die EU: BoD - Books on Demand, In de Tarpen 42, 22848 Norderstedt, info[at]bod[dot]de | Anbieter: preigu.…

Condizione: As New. Unread book in perfect condition.

Paperback. Condizione: Like New. LIKE NEW. SHIPS FROM MULTIPLE LOCATIONS. book.

Condizione: As New. Unread book in perfect condition.

paperback. Condizione: New. NEW. SHIPS FROM MULTIPLE LOCATIONS. book.

paperback. Condizione: New. NEW. SHIPS FROM MULTIPLE LOCATIONS. book.

Condizione: New.

Condizione: New.

Condizione: New. In English.

Taschenbuch. Condizione: Neu. Stressabbauprüfungen und stabilitätsanzeigende Analysemethoden | Stressabbaustudien, stabilitätsindizierende Analysemethoden, HPLC, HPTLC-Analyse, Verunreinigungen | Mirza Shahed Baig | Taschenbuch | 368 S. | Deutsch | 2023 | Verlag Unser Wissen | EAN 9786205666500 | Verantwortliche Person für die EU: SIA OmniScriptum Publishing, Brivibas Gatve 197, 1039 RIGA, LETTLAND, customerservice[at]vdm-vsg[dot]de | Anbieter: preigu.…

paperback. Condizione: New. NEW. SHIPS FROM MULTIPLE LOCATIONS. book.

PAP. Condizione: New. New Book. Shipped from UK. THIS BOOK IS PRINTED ON DEMAND. Established seller since 2000.

PAP. Condizione: New. New Book. Delivered from our UK warehouse in 4 to 14 business days. THIS BOOK IS PRINTED ON DEMAND. Established seller since 2000.

Condizione: New. Dieser Artikel ist ein Print on Demand Artikel und wird nach Ihrer Bestellung fuer Sie gedruckt. Autor/Autorin: Fatima Khan SamreenMs. Khan Samreen fatima. Master of pharmacy (Quality Assurance) from YB chavan college of pharmacy, Aurangabad. Maharashtra.Regadenoson is a drug which is presently in the form of IV to increase blood flow in a.…

Kartoniert / Broschiert. Condizione: New. Dieser Artikel ist ein Print on Demand Artikel und wird nach Ihrer Bestellung fuer Sie gedruckt. Autor/Autorin: Khan HajeraHajera Khan has obtained M.Pharmacy in Quality Assurance in 2011.Presently she is working as asst.professor.She is author of several articles published in national and international journals.Gemifloxacin,a flouroquino.…

Condizione: New. Print on Demand pp. 124 2:B&W 6 x 9 in or 229 x 152 mm Perfect Bound on Creme w/Gloss Lam.

Condizione: New. PRINT ON DEMAND pp. 124.

Taschenbuch. Condizione: Neu. This item is printed on demand - it takes 3-4 days longer - Neuware -Quality of any Active Pharmaceutical Ingredient (API) or drug product for patient compliance is directly depending on stability of drug. The ICH drug stability test guideline Q1A (R2) requires that analysis of stability samples should be done through the use of validated Stability indicating assay methods (SIAMs) that can detect the changes with time in the chemical, physical, or microbiological properties of the drug substance and drug product, and that are specific, so that the contents of active ingredient, degradation products, and other components of interest can be accurately measured without interference. A proactive approach in developing a SIAMs involve forced degradation at the early stages of development with the key degradation samples used in the method development process. 428 pp. Englisch.…

Taschenbuch. Condizione: Neu. nach der Bestellung gedruckt Neuware - Printed after ordering - Quality of any Active Pharmaceutical Ingredient (API) or drug product for patient compliance is directly depending on stability of drug. The ICH drug stability test guideline Q1A (R2) requires that analysis of stability samples should be done through the use of validated Stability indicating assay methods (SIAMs) that can detect the changes with time in the chemical, physical, or microbiological properties of the drug substance and drug product, and that are specific, so that the contents of active ingredient, degradation products, and other components of interest can be accurately measured without interference. A proactive approach in developing a SIAMs involve forced degradation at the early stages of development with the key degradation samples used in the method development process.…

Taschenbuch. Condizione: Neu. This item is printed on demand - Print on Demand Titel. Neuware -Quality of any Active Pharmaceutical Ingredient (API) or drug product for patient compliance is directly depending on stability of drug. The ICH drug stability test guideline Q1A (R2) requires that analysis of stability samples should be done through the use of validated Stability indicating assay methods (SIAMs) that can detect the changes with time in the chemical, physical, or microbiological properties of the drug substance and drug product, and that are specific, so that the contents of active ingredient, degradation products, and other components of interest can be accurately measured without interference. A proactive approach in developing a SIAMs involve forced degradation at the early stages of development with the key degradation samples used in the method development process.VDM Verlag, Dudweiler Landstraße 99, 66123 Saarbrücken 428 pp. Englisch.…

Taschenbuch. Condizione: Neu. This item is printed on demand - it takes 3-4 days longer - Neuware -La calidad de cualquier Ingrediente Farmacéutico Activo (API) o producto farmacéutico para el cumplimiento de los pacientes depende directamente de la estabilidad del fármaco. La directriz Q1A (R2) sobre pruebas de estabilidad de fármacos de la ICH exige que el análisis de las muestras de estabilidad se realice mediante el uso de métodos de ensayo indicadores de estabilidad (SIAM) validados que puedan detectar los cambios con el tiempo en las propiedades químicas, físicas o microbiológicas de la sustancia y el producto farmacéuticos, y que sean específicos, de modo que el contenido del principio activo, los productos de degradación y otros componentes de interés puedan medirse con precisión sin interferencias. Un enfoque proactivo en el desarrollo de un SIAM implica la degradación forzada en las primeras etapas de desarrollo con las muestras clave de degradación utilizadas en el proceso de desarrollo del método. 356 pp. Spanisch. …

Taschenbuch. Condizione: Neu. nach der Bestellung gedruckt Neuware - Printed after ordering - La calidad de cualquier Ingrediente Farmacéutico Activo (API) o producto farmacéutico para el cumplimiento de los pacientes depende directamente de la estabilidad del fármaco. La directriz Q1A (R2) sobre pruebas de estabilidad de fármacos de la ICH exige que el análisis de las muestras de estabilidad se realice mediante el uso de métodos de ensayo indicadores de estabilidad (SIAM) validados que puedan detectar los cambios con el tiempo en las propiedades químicas, físicas o microbiológicas de la sustancia y el producto farmacéuticos, y que sean específicos, de modo que el contenido del principio activo, los productos de degradación y otros componentes de interés puedan medirse con precisión sin interferencias. Un enfoque proactivo en el desarrollo de un SIAM implica la degradación forzada en las primeras etapas de desarrollo con las muestras clave de degradación utilizadas en el proceso de desarrollo del método.…