【召集人專欄】<藥物安全系列五> 藥廠的藥物安全事件處理流程(下) (Liang-Ni Wu)
After triage, the case may enter the processing step. The purpose of case processing is to ensure a standard and structured way to capture the case information in the safety database.
生醫專欄
After triage, the case may enter the processing step. The purpose of case processing is to ensure a standard and structured way to capture the case information in the safety database.
In my last article in December 2016, I introduced about the pharmacovigilance system to be set up by pharmaceutical companies and one of the key elements being a quality system describing the procedures.
In my last article in October 2016, I used an example to discuss whether efficacy or safety comes first in the aspect of drug development. I would like to share Shyam Krishnan’s response, which well summarizes that pharmaceutical...
橘皮書(The Orange Book)是由美國食品藥物管理局FDA官方出版的書冊,正式名稱為「具治療等效性評估之核准藥品目錄(Approved Drug Products with Therapeutic Equivalences)」,登錄包含經FDA核准上市藥品之專利資訊...
資料專屬權(Data Exclusivity )是指原廠(第一個新藥開發廠)提出新藥上市申請時,所檢具證明安全性及療效之各種相關申請資料,其他藥商非經原廠同意,於法定之保護期間內不得引用,簡而言之,就是行政機關針對原廠新藥上市申請資料給予的行政保護權。
Further to my Introduction to Drug Safety Series posted in August 2016, I did not expect to a hot discussion over this not-so-popular topic. Indeed, there were only two comments posted - but I was surprised, and quite amazed to read these comments...
我們到醫院診所領藥,藥師需要三讀三對,才能讓患者領到這些醫師開的處方籤。然而當消費者吃到這顆藥之前,藥廠要生產這些藥品,可是需要經過相當嚴謹的法規管制。
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