Importance and globalization status of good manufacturing practice (GMP) requirements for pharmaceutical excipients
نام نخستين پديدآور
/ Abubaker Abdellah
نام ساير پديدآوران
; Mohamed Ibrahim Noordin, Wan Azman Wan Ismail
يادداشت کلی
متن يادداشت
REVIEW
یادداشتهای مربوط به خلاصه یا چکیده
متن يادداشت
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.
قطعه
عنوان
Saudi Pharmaceutical Journal
شماره جلد
, Volume 23, Issue 1
تاريخ نشر
, January 2015
توصيف ظاهري
: P. 9-13
موضوع (اسم عام یاعبارت اسمی عام)
موضوع مستند نشده
Globalization
موضوع مستند نشده
Importance of pharmaceutical excipients
موضوع مستند نشده
Good manufacturing practice
موضوع مستند نشده
Excipient’s evaluation
موضوع مستند نشده
Excipient’s Safety
نام شخص به منزله سر شناسه - (مسئولیت معنوی درجه اول )