Feasibility of manufaturing a suppository by compressing with different proportions of excipients in comparison to existing formula

Diplôme Master Feasibility of manufaturing a suppository by compressing with different proportions of excipients in comparison to existing formula eng 2012 author Wydmanska Broch Edyta 676155 director Guizani Samd director Rudaz Serge 0000-0002-4180-5417 28978 director Allémann Eric 0000-0002-6598-9521 26730 According to the ICH harmonized guidelines, the aim of pharmaceutical development is to design a quality product and its manufacturing process to consistently deliver the intended performance of the product. The information and knowledge gained from pharmaceutical development studies and manufacturing experience provide scientific understanding to support the establishment of the design space, specifications, and manufacturing controls [1]. The design space is a multidimensional combination and interaction of input variables and process parameters that have been demonstrated to provide assurance of quality. Design space is proposed by the applicant and is subjected to regulatory assessment and approval [1]. Dewey 615 Master in Pharmacy - Travail personnel de recherche 31 Section des sciences pharmaceutiques 17 false 57e92728-92fe-43dd-a88f-006163fb6631 Master thesis Restricted Edyta Wydmanska, Travail de Master.pdf 1722279 application/pdf restrictedAccess Faculté des sciences / Section des sciences pharmaceutiques

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Feasibility of manufaturing a suppository by compressing with different proportions of excipients in comparison to existing formula				2012	316	0

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Wydmanska Broch, Edyta