کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
2509209 1117653 2015 5 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Importance and globalization status of good manufacturing practice (GMP) requirements for pharmaceutical excipients
موضوعات مرتبط
علوم پزشکی و سلامت داروسازی، سم شناسی و علوم دارویی علوم دارویی
پیش نمایش صفحه اول مقاله
Importance and globalization status of good manufacturing practice (GMP) requirements for pharmaceutical excipients
چکیده انگلیسی

Pharmaceutical excipients are no longer inert materials but it is effective and able to improve the characteristics of the products’ quality, stability, functionality, safety, solubility and acceptance of patients. It can interact with the active ingredients and alter the medicament characteristics. The globalization of medicines’ supply enhances the importance of globalized good manufacturing practice (GMP) requirements for pharmaceutical excipients. This review was intended to assess the globalization status of good manufacturing practice (GMP) requirements for pharmaceutical excipients. The review outcomes demonstrate that there is a lack of accurately defined methods to evaluate and measure excipients’ safety. Furthermore good manufacturing practice requirements for excipients are not effectively globalized.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Saudi Pharmaceutical Journal - Volume 23, Issue 1, January 2015, Pages 9–13
نویسندگان
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