l*********g
发帖数: 94 | | h*******o
发帖数: 4884 | 2 前者是后者涵盖的一部分
【在 l*********g 的大作中提到】
: 哪位前辈给比较比较。
| l*********g
发帖数: 94 | 3 哦，涨知识了。那这两个方向上有哪些公认的证书课程么？
【在 h*******o 的大作中提到】
: 前者是后者涵盖的一部分
| j******w
发帖数: 97 | 4 PV is focused on adverse event reporting and analysis, generally requires
some type of clinical experience, such as nursing.
Regulatory affairs is broader.
Go to indeed.com and search for pharmacovigilance jobs,you will get some
idea what type of responsibilities PV assumes.
Regulatory affairs has several major sub-areas, clinical, CMC, global,
submission management, labeling, ad/prom. It is a little tricky to get a
good understanding of the responsibilities. So try to find a "generalist/
strategist" type of job that requires everything. | b*****s
发帖数: 297 | 5 PV对中国人容易些，而且我觉得这帮人整天屁事没有。就搞点AE，半年搞一次，都是重
复性的，不要太轻松
★ 发自iPhone App: ChineseWeb 8.6
【在 l*********g 的大作中提到】
: 哪位前辈给比较比较。
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