International Pharmaceutical Product Registration 在线电子书 pdf 下载 txt下载 epub 下载 mobi 下载 2024

☆☆☆☆☆
简体网页||繁体网页

Cartwright, Tony (EDT)/ Matthews, Brian (EDT) 作者

译者

2009-8 出版日期

852 页数

$ 536.75 价格

丛书系列

9781420081763 图书编码

International Pharmaceutical Product Registration 在线电子书图书标签:

喜欢 International Pharmaceutical Product Registration 在线电子书的读者还喜欢

下载链接在页面底部

点击这里下载

想要找书就要到图书目录大全

book.wenda123.org

立刻按 ctrl+D收藏本页

你会得到大惊喜!!

发表于2024-12-27

facebook linkedin mastodon messenger pinterest reddit telegram twitter viber vkontakte whatsapp 复制链接

International Pharmaceutical Product Registration 在线电子书 epub 下载 mobi 下载 pdf 下载 txt 下载 2024

International Pharmaceutical Product Registration 在线电子书 pdf 下载 txt下载 epub 下载 mobi 下载 2024

International Pharmaceutical Product Registration 在线电子书用户评价

评分☆☆☆☆☆

International Pharmaceutical Product Registration 在线电子书著者简介

International Pharmaceutical Product Registration 在线电子书图书目录

International Pharmaceutical Product Registration 在线电子书 pdf 下载 txt下载 epub 下载 mobi 在线电子书下载

International Pharmaceutical Product Registration 在线电子书图书描述

Top international regulatory experts, scientists, and clinicians deliver the much-needed information that regulatory affairs professionals and drug development scientists need for registering new products. With harmonization discussions and negotiations in full swing between the major regulatory agencies and pharmaceutical trade associations in the US, Japan, and Europe, this Second Edition is an essential guide for all who need to be kept abreast of developments since the first edition. Key benefits include: ICH GUIDELINES-established at the International Conference on Harmonization (ICH) in the areas of Quality, Safety, Efficacy, and Multidisciplinary, which need to be taken into account are discussed, in detail PROGRESS ON HARMONIZATION-including the increased cooperation between agencies, based on ICH, as well as accepted derivatives of the Common Technical Document (CTD), that can lead to time and cost-savings in the product registration process CONTRIBUTIONS FROM 45 EXPERTS-with broad expertise and knowledge of the scientific and technical requirements involved in drug regulation provide authoritative advice and viewpoints you can trust BENEFITS OF OUTSOURCING RESEARCH AND CLINICAL TRIALS-made possible by the existence of internationally accepted guidelines, gives you access to well-trained physicians and a larger, more diverse sample market at a lower cost

International Pharmaceutical Product Registration 在线电子书下载 mobi epub pdf txt 在线电子书下载

想要找书就要到图书目录大全

book.wenda123.org

立刻按 ctrl+D收藏本页

你会得到大惊喜!!