The Twenty-four Books of the Holy Scriptures PDF Download

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The Twenty-four Books of the Holy Scriptures

The Twenty-four Books of the Holy Scriptures PDF Author: Isaac Leeser
Publisher:
ISBN:
Category :
Languages : en
Pages : 1266

Book Description


The Twenty-four Books of the Holy Scriptures

The Twenty-four Books of the Holy Scriptures PDF Author: Isaac Leeser
Publisher:
ISBN:
Category :
Languages : en
Pages : 1266

Book Description


Pharmaceutical Dosage Forms

Pharmaceutical Dosage Forms PDF Author: Herbert Lieberman
Publisher: CRC Press
ISBN: 1000148416
Category : Medical
Languages : en
Pages : 558

Book Description
Stressing the theory involved in formulating suspensions, emulsions, and colloidal drug products, this Second Edition of a well-received reference test highlights typical formulations, the avoidance of formulation pitfalls, and compliance with established regulatory principles.

From Ridge to River

From Ridge to River PDF Author: United States. Soil Conservation Service
Publisher:
ISBN:
Category : Soil conservation
Languages : en
Pages : 16

Book Description


Panjab Gazetteer

Panjab Gazetteer PDF Author:
Publisher:
ISBN:
Category :
Languages : en
Pages : 620

Book Description


Pharmaceutical Suspensions

Pharmaceutical Suspensions PDF Author: Alok K. Kulshreshtha
Publisher: Springer Science & Business Media
ISBN: 1441910875
Category : Medical
Languages : en
Pages : 337

Book Description
The suspension dosage form has long been used for poorly soluble active ingre- ents for various therapeutic indications. Development of stable suspensions over the shelf life of the drug product continues to be a challenge on many fronts. A good understanding of the fundamentals of disperse systems is essential in the development of a suitable pharmaceutical suspension. The development of a s- pension dosage form follows a very complicated path. The selection of the proper excipients (surfactants, viscosity imparting agents etc.) is important. The particle size distribution in the finished drug product dosage form is a critical parameter that significantly impacts the bioavailability and pharmacokinetics of the product. Appropriate analytical methodologies and instruments (chromatographs, visco- ters, particle size analyzers, etc.) must be utilized to properly characterize the s- pension formulation. The development process continues with a successful scale-up of the manufacturing process. Regulatory agencies around the world require cli- cal trials to establish the safety and efficacy of the drug product. All of this devel- ment work should culminate into a regulatory filing in accordance with the regulatory guidelines. Pharmaceutical Suspensions, From Formulation Development to Manufacturing, in its organization, follows the development approach used widely in the pharmaceutical industry. The primary focus of this book is on the classical disperse system – poorly soluble active pharmaceutical ingredients s- pended in a suitable vehicle.