Vyas niraj (60 resultados)

Paperback. Condición: Brand New. 60 pages. 8.66x5.91x0.14 inches. In Stock.

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Taschenbuch. Condición: Neu. Stability Indicating HPTLC Method for Estimation of Ursolic Acid | Niraj Vyas (u. a.) | Taschenbuch | 60 S. | Englisch | 2015 | LAP LAMBERT Academic Publishing | EAN 9783659625909 | Verantwortliche Person für die EU: preigu GmbH & Co. KG, Lengericher Landstr. 19, 49078 Osnabrück, mail[at]preigu[dot]de | Anbieter: preigu.…

Condición: New.

Condición: New.

Condición: New.

Condición: New.

Taschenbuch. Condición: Neu. This item is printed on demand - it takes 3-4 days longer - Neuware -Stability of a pharmaceutical product is defined as the capability of a particular formulation in a specific container/closure system to remain within its physical, chemical, microbiological, toxicological, protective and informational specifications. Thus it is very important to ensure that a raw material/finished product must be stable during the period of use and its storage. Stability testing of pharmaceutical products is a set of procedures ensuring quality, efficacy and safety in a raw material and finished formulation. Stability testing is an important requirement for regulatory approval of any drug in many countries. Generally herbal products are considered as safe. It is a myth. Various countries have limited use of plant based formulations because of lack of its stability, safety, efficacy and toxicity data. This work describes the stability testing of one such phyto constituent Ursolic acid according to ICH guideline. This work can help future studies of such type for other compounds of plant origin and to document the proof of its safety, efficacy and stability in the favour of patient compliance. 60 pp. Englisch. …

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

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

Taschenbuch. Condición: Neu. nach der Bestellung gedruckt Neuware - Printed after ordering - Stability of a pharmaceutical product is defined as the capability of a particular formulation in a specific container/closure system to remain within its physical, chemical, microbiological, toxicological, protective and informational specifications. Thus it is very important to ensure that a raw material/finished product must be stable during the period of use and its storage. Stability testing of pharmaceutical products is a set of procedures ensuring quality, efficacy and safety in a raw material and finished formulation. Stability testing is an important requirement for regulatory approval of any drug in many countries. Generally herbal products are considered as safe. It is a myth. Various countries have limited use of plant based formulations because of lack of its stability, safety, efficacy and toxicity data. This work describes the stability testing of one such phyto constituent Ursolic acid according to ICH guideline. This work can help future studies of such type for other compounds of plant origin and to document the proof of its safety, efficacy and stability in the favour of patient compliance. …

Condición: New. Dieser Artikel ist ein Print on Demand Artikel und wird nach Ihrer Bestellung fuer Sie gedruckt. Autor/Autorin: Vyas NirajMr. Niraj Vyas is Post Graduate in Phytopharmaceuticals and Natural Products. He is a gold Medalist in his PG studies. His research areas includes Development and method validation for estimation of herbal compounds in raw .…

Paperback. Condición: new. Paperback. La stabilite d'un produit pharmaceutique est definie comme la capacite d'une formulation donnee, dans un systeme specifique de conditionnement (recipient et bouchon), a rester conforme a ses specifications physiques, chimiques, microbiologiques, toxicologiques, de protection et d'information. Il est donc essentiel de s'assurer qu'une matiere premiere ou un produit fini reste stable pendant toute la duree de son utilisation et de son stockage. Les essais de stabilite des produits pharmaceutiques constituent un ensemble de procedures visant a garantir la qualite, l'efficacite et la securite d'une matiere premiere et d'une formulation finie. Ces essais constituent une exigence importante pour l'autorisation de mise sur le marche de tout medicament dans de nombreux pays. Les produits a base de plantes sont generalement consideres comme surs. Il s'agit la d'un mythe. Plusieurs pays ont restreint l'utilisation des formulations a base de plantes en raison du manque de donnees sur leur stabilite, leur innocuite, leur efficacite et leur toxicite. Ce travail decrit les essais de stabilite d'un de ces constituants vegetaux, l'acide ursolique, conformement aux lignes directrices de l'ICH. Ce travail peut contribuer a de futures etudes de ce type portant sur d'autres composes d'origine vegetale et permettre de documenter la preuve de leur innocuite, de leur efficacite et de leur stabilite, dans l'interet de l'observance therapeutique des patients. This item is printed on demand. Shipping may be from multiple locations in the US or from the UK, depending on stock availability. …

Taschenbuch. Condición: Neu. This item is printed on demand - it takes 3-4 days longer - Neuware 56 pp. Spanisch.

Taschenbuch. Condición: Neu. This item is printed on demand - Print on Demand Titel. Neuware -Stability of a pharmaceutical product is defined as the capability of a particular formulation in a specific container/closure system to remain within its physical, chemical, microbiological, toxicological, protective and informational specifications. Thus it is very important to ensure that a raw material/finished product must be stable during the period of use and its storage. Stability testing of pharmaceutical products is a set of procedures ensuring quality, efficacy and safety in a raw material and finished formulation. Stability testing is an important requirement for regulatory approval of any drug in many countries. Generally herbal products are considered as safe. It is a myth. Various countries have limited use of plant based formulations because of lack of its stability, safety, efficacy and toxicity data. This work describes the stability testing of one such phyto constituent Ursolic acid according to ICH guideline. This work can help future studies of such type for other compounds of plant origin and to document the proof of its safety, efficacy and stability in the favour of patient compliance.VDM Verlag, Dudweiler Landstraße 99, 66123 Saarbrücken 60 pp. Englisch. …

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

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

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

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

Taschenbuch. Condición: Neu. This item is printed on demand - it takes 3-4 days longer - Neuware 56 pp. Französisch.

Taschenbuch. Condición: Neu. nach der Bestellung gedruckt Neuware - Printed after ordering - La estabilidad de un producto farmacéutico se define como la capacidad de una formulación concreta, en un sistema específico de envase y cierre, para mantenerse dentro de sus especificaciones físicas, químicas, microbiológicas, toxicológicas, de protección e informativas. Por lo tanto, es muy importante garantizar que una materia prima o un producto terminado sea estable durante su periodo de uso y almacenamiento. Los ensayos de estabilidad de los productos farmacéuticos constituyen un conjunto de procedimientos que garantizan la calidad, la eficacia y la seguridad de una materia prima y de una formulación terminada. Los ensayos de estabilidad son un requisito importante para la autorización reglamentaria de cualquier medicamento en muchos países. Por lo general, se considera que los productos a base de plantas son seguros. Esto es un mito. Varios países han restringido el uso de formulaciones de origen vegetal debido a la falta de datos sobre su estabilidad, seguridad, eficacia y toxicidad. Este trabajo describe los ensayos de estabilidad de uno de estos fitoconstituyentes, el ácido ursólico, de acuerdo con las directrices de la ICH. Este trabajo puede contribuir a futuros estudios de este tipo para otros compuestos de origen vegetal y a documentar la prueba de su seguridad, eficacia y estabilidad, en beneficio del cumplimiento terapéutico de los pacientes. …

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

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

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

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

Paperback. Condición: new. Paperback. A estabilidade de um produto farmaceutico define-se como a capacidade de uma determinada formulacao, num sistema especifico de embalagem/fecho, de se manter dentro das suas especificacoes fisicas, quimicas, microbiologicas, toxicologicas, de protecao e informativas. Assim, e muito importante garantir que uma materia-prima ou um produto acabado se mantenha estavel durante o periodo de utilizacao e armazenamento. Os ensaios de estabilidade de produtos farmaceuticos constituem um conjunto de procedimentos que garantem a qualidade, a eficacia e a seguranca de uma materia-prima e de uma formulacao acabada. Os ensaios de estabilidade sao um requisito importante para a aprovacao regulamentar de qualquer medicamento em muitos paises. Geralmente, os produtos a base de plantas sao considerados seguros. Trata-se de um mito. Varios paises restringiram a utilizacao de formulacoes a base de plantas devido a falta de dados relativos a sua estabilidade, seguranca, eficacia e toxicidade. Este trabalho descreve os ensaios de estabilidade de um desses fito-constituintes, o acido ursolico, de acordo com as diretrizes da ICH. Este trabalho pode contribuir para futuros estudos deste tipo relativos a outros compostos de origem vegetal e para documentar a comprovacao da sua seguranca, eficacia e estabilidade, a favor da adesao do doente ao tratamento. This item is printed on demand. Shipping may be from multiple locations in the US or from the UK, depending on stock availability.…

Paperback. Condición: new. Paperback. Stabilnosc produktu farmaceutycznego definiuje sie jako zdolnosc danej postaci leku w okreslonym systemie opakowania i zamkniecia do zachowania zgodnosci z wymaganiami specyfikacji fizycznych, chemicznych, mikrobiologicznych, toksykologicznych, ochronnych i informacyjnych. Dlatego niezwykle wazne jest zapewnienie, aby surowiec lub gotowy produkt zachowywal stabilnosc w okresie stosowania i przechowywania. Badania stabilnosci produktow farmaceutycznych to zestaw procedur zapewniajacych jakosc, skutecznosc i bezpieczenstwo surowca oraz gotowego preparatu. Badania stabilnosci sa waznym wymogiem dla uzyskania zezwolenia regulacyjnego na dopuszczenie do obrotu dowolnego leku w wielu krajach. Ogolnie uwaza sie, ze produkty ziolowe sa bezpieczne. Jest to jednak mit. W wielu krajach stosowanie preparatow pochodzenia roslinnego jest ograniczone ze wzgledu na brak danych dotyczacych ich stabilnosci, bezpieczenstwa, skutecznosci i toksycznosci. Niniejsza praca opisuje badania stabilnosci jednego z takich skladnikow roslinnych - kwasu ursolowego - zgodnie z wytycznymi ICH. Praca ta moze pomoc w przyszlych badaniach tego typu dotyczacych innych zwiazkow pochodzenia roslinnego oraz w udokumentowaniu dowodow na ich bezpieczenstwo, skutecznosc i stabilnosc, co sprzyja przestrzeganiu zalecen przez pacjentow. This item is printed on demand. Shipping may be from multiple locations in the US or from the UK, depending on stock availability.…

Paperback. Condición: new. Paperback. Die Stabilitaet eines Arzneimittels ist definiert als die Faehigkeit einer bestimmten Formulierung in einem spezifischen Behaelter-/Verschlusssystem, die physikalischen, chemischen, mikrobiologischen, toxikologischen, schutztechnischen und informativen Spezifikationen einzuhalten. Daher ist es aeusserst wichtig, sicherzustellen, dass ein Rohstoff bzw. ein Fertigarzneimittel waehrend der Verwendungsdauer und der Lagerung stabil bleibt. Stabilitaetspruefungen von Arzneimitteln umfassen eine Reihe von Verfahren, die die Qualitaet, Wirksamkeit und Sicherheit eines Rohstoffs und einer fertigen Formulierung gewaehrleisten. Stabilitaetspruefungen sind in vielen Laendern eine wichtige Voraussetzung fuer die behoerdliche Zulassung eines Arzneimittels. Im Allgemeinen gelten pflanzliche Produkte als sicher. Dies ist jedoch ein Mythos. In verschiedenen Laendern ist die Verwendung pflanzlicher Praeparate aufgrund fehlender Daten zu Stabilitaet, Sicherheit, Wirksamkeit und Toxizitaet eingeschraenkt. Diese Arbeit beschreibt die Stabilitaetspruefung eines solchen pflanzlichen Wirkstoffs, der Ursolsaeure, gemaess der ICH-Richtlinie. Diese Arbeit kann zukuenftige Studien dieser Art fuer andere pflanzliche Verbindungen unterstuetzen und dazu beitragen, den Nachweis ihrer Sicherheit, Wirksamkeit und Stabilitaet zu dokumentieren, was der Therapietreue der Patienten zugutekommt. This item is printed on demand. Shipping may be from multiple locations in the US or from the UK, depending on stock availability.…

Paperback. Condición: new. Paperback. La stabilita di un prodotto farmaceutico e definita come la capacita di una particolare formulazione, all'interno di uno specifico sistema contenitore/chiusura, di rimanere entro i limiti delle specifiche fisiche, chimiche, microbiologiche, tossicologiche, protettive e informative. E quindi fondamentale garantire che una materia prima o un prodotto finito sia stabile durante il periodo di utilizzo e di conservazione. I test di stabilita dei prodotti farmaceutici costituiscono una serie di procedure volte a garantire la qualita, l'efficacia e la sicurezza sia della materia prima che della formulazione finita. I test di stabilita rappresentano un requisito fondamentale per l'approvazione normativa di qualsiasi farmaco in molti paesi. Generalmente i prodotti a base di erbe sono considerati sicuri. Si tratta pero di un mito. Diversi paesi hanno limitato l'uso di formulazioni a base vegetale a causa della mancanza di dati relativi alla loro stabilita, sicurezza, efficacia e tossicita. Il presente lavoro descrive i test di stabilita di uno di questi costituenti fitochimici, l'acido ursolico, secondo le linee guida ICH. Questo lavoro puo contribuire a futuri studi di questo tipo su altri composti di origine vegetale e a documentare la prova della loro sicurezza, efficacia e stabilita a favore dell'aderenza terapeutica dei pazienti. This item is printed on demand. Shipping may be from multiple locations in the US or from the UK, depending on stock availability. …

Taschenbuch. Condición: Neu. This item is printed on demand - Print on Demand Titel. Neuware 56 pp. Spanisch.