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Prashar, Deepak
- Pharmaco-Economical Overview of Natural Gums and Hydrocolloids
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Authors
Affiliations
1 Department of Economics, Govt. College, Dharampur, Mandi (H.P.), IN
2 Department of Pharmaceutical Sciences, Vinayaka College of Pharmacy, Kullu (H.P.), IN
1 Department of Economics, Govt. College, Dharampur, Mandi (H.P.), IN
2 Department of Pharmaceutical Sciences, Vinayaka College of Pharmacy, Kullu (H.P.), IN
Source
Research Journal of Pharmaceutical Dosage Form and Technology, Vol 4, No 5 (2012), Pagination: 256-259Abstract
When it comes to drug delivery system, coating with the polymer had been an important prospect. The availability of polymer in both biodegradable and non-biodegradable forms provides an added advantage of modification. In the current scenario, the quality of the product has to be in good economical range. The good quality of the preparation or formulation may inspire the consumer; however the economical aspect finally ends up in buying the product. Thus the study of pharmaco-economical aspects becomes an important criterion. The gums and hydrocolloids had been recommended in pharmacy for various purposes, yet its use and demand depends upon its economical overview.
Keywords
Gums, Hydrocolloids, Economics, Polymers.- Process Validation: An Overview
Abstract Views :198 |
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Authors
Affiliations
1 Department of Pharmaceutical Sciences, Manav Bharti University, Solan (H.P.), IN
1 Department of Pharmaceutical Sciences, Manav Bharti University, Solan (H.P.), IN
Source
Research Journal of Pharmaceutical Dosage Form and Technology, Vol 3, No 6 (2011), Pagination: 247-250Abstract
Validation is an act of demonstrating a procedure, process, and activity which will consistently lead to the expected results. In pharmaceuticals there are wide varieties of procedures and processes which need to be validated. The validation process consists of identifying and testing all aspects of a process that could affect the final test or product. Prior to the testing of a process, the system must be properly qualified. A properly designed system will provide a high degree of assurance in order to evaluate every step, process and change before its implementation. In this paper, statistical issues, regulatory requirements required for process validation options in drug development are discussed.Keywords
Process Validation, cGMPs, Pilot Scale-Up, Validation Options, Statistical Issues.- Pharmaceutical and Economical Aspects of Porous Tablets
Abstract Views :193 |
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Authors
Affiliations
1 Department of Pharmaceutical Sciences, Manav Bharti University, Solan (H.P.), IN
2 Department of Economics, Govt. College Dharampur, Mandi (H.P.), IN
3 Department of Pharmaceutical Sciences, Manav Bharti University, Solan (H.P.), IN
1 Department of Pharmaceutical Sciences, Manav Bharti University, Solan (H.P.), IN
2 Department of Economics, Govt. College Dharampur, Mandi (H.P.), IN
3 Department of Pharmaceutical Sciences, Manav Bharti University, Solan (H.P.), IN