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    [热点] 读博 17制药周凯 2025-12-17 刚刚
    [关贴]文献密码搜索的方法大全 (2/215) hexinhua0920 2007-04-21 2007-04-21 21:36:57 by borall
    [注册申报] 国内4类新药注册程序 (4/699) beibei4891 2007-04-13 2007-04-21 14:39:10 by beibei4891
    [政策法规] 《药品注册管理办法》修订征求意见座谈会 (0/138) lwjxz 2007-04-21 2007-04-21 13:29:14 by lwjxz
    [资料求助] 求助氯诺昔康片质量标准 (3/239) lufuqiang 2007-04-21 2007-04-21 11:29:53 by lufuqiang
    [快捷药讯] 新产品上市手册 (3/345) gcjgoat 2007-04-01 2007-04-21 11:06:14 by chenminchun
    [快捷药讯] 增加药用辅料的厂家 (1/125) jyc0571 2007-04-21 2007-04-21 09:48:58 by 豆哥
    [注册申报] 注册办法修订座谈会(转帖) (0/107) shinhwabest 2007-04-21 2007-04-21 08:55:23 by shinhwabest
    [资料求助] 求助：不知哪位有1999年德国药典？谢谢！ (0/196) lylghlhp 2007-04-21 2007-04-21 08:14:37 by lylghlhp
    [资料求助] 求助 (9/200) maidisen 2007-04-16 2007-04-20 18:59:45 by 小小强
    [政策法规] 求助:注射剂改变规格 (1/88) shinhwabest 2007-04-19 2007-04-20 18:43:38 by 小小强
    [快捷药讯] [关贴]急求二手研发实验室仪器设备（整体转让） (0/351) liweihong74 2007-04-20 2007-04-20 17:12:10 by liweihong74
    [质量控制] 求助：药品中添加色素有什么要求？ (2/201) wking0257069 2007-04-19 2007-04-20 16:37:39 by wking0257069
    [政策法规] 药品核查工作延长到2007年底--223号文 (7/568) 药巫 2007-04-19 2007-04-20 14:11:24 by xch1100
    [资料求助] 求助：申报表查询 (2/102) gtt100102 2007-04-19 2007-04-20 11:24:26 by gtt100102
    [政策法规] [求助]关于dropbox存取码的获取方法 (0/73) robbiekean 2007-04-20 2007-04-20 10:58:28 by robbiekean
    [注册申报] 各国的药物不良反应报表 (0/284) gtt100102 2007-04-20 2007-04-20 09:32:17 by gtt100102
    [质量控制] 欧盟认证的请进 (2/141) ylyyxyc 2007-04-19 2007-04-20 08:34:03 by jjm_0451
    [资料求助] 求助，谁能买到尿酸啊 (0/150) zuofang 2007-04-19 2007-04-19 22:31:57 by zuofang
    [快捷药讯] [关贴]氢气 (1/226) zpfzgz 2007-04-04 2007-04-19 20:24:45 by nauvet
    [质量控制] 2003--2020年到期专利 (3/277) yuyu19831124 2007-04-19 2007-04-19 20:22:57 by gter_wang
    有什么好得抗艾滋病得 (0/72) DMFluhui 2007-04-19 2007-04-19 19:26:15 by DMFluhui
    罗红胶囊－胶囊填充困难 (6/452) dsonghao 2007-04-14 2007-04-19 17:41:58 by muzili327846
    关于按24号文修订说明书的疑点? (5/421) workyx 2007-04-12 2007-04-19 15:17:43 by cuixuguang
    [质量控制] 【转帖】GMP后遗症陕西药企负债30亿 (8/620) forbbs 2007-04-12 2007-04-19 14:52:03 by cuixuguang
    [资料求助] 投票:  新药发版候选斑竹有奖投票调查，欢迎大家积极参与！已经结束，谢谢大家。    ( 1 2 3 4 5 ) (41/1370) 小小强 2007-03-28 2007-04-19 14:26:22 by 5安然
    关于药物“溶出度”的测定方法 (金币≥1)(4/135) workyx 2007-04-18 2007-04-19 14:18:06 by jiaban
    [快捷药讯] 【求助】蝙蝠蛾拟青霉的质量标准 (7/1452) manrmoon 2007-04-16 2007-04-19 11:52:37 by manrmoon
    新药研究中在哪些地方可以查到以前药物的半数致死量如地塞米松 (2/424) carefreewu 2007-04-18 2007-04-19 11:12:31 by carefreewu
    [质量控制] 欧洲水的标准 (1/97) DMFluhui 2007-04-18 2007-04-19 00:35:21 by kevinhh
    [快捷药讯] 冬虫夏草人工孕育难题被攻克 (8/746) liuxm123 2007-03-23 2007-04-18 23:01:23 by buck2004
    如何查找某个具体新药的具体药学信息 (4/518) vicardin 2007-01-12 2007-04-18 20:23:17 by DMFluhui
    [资料求助] [分享]植物化工行业招聘信息 (1/115) fanganbin 2007-04-18 2007-04-18 17:58:41 by 豆哥
    [政策法规] 化学药研究指导原则 (金币≥5)(3/97) hexinhua0920 2007-04-17 2007-04-18 13:03:17 by 小小强
    [快捷药讯] me-too 药物？如何运用！请高手赐教！ (金币≥2)(8/205) wchao612 2007-03-12 2007-04-18 10:43:53 by bybqd
    [政策法规] [转]“863”生物和医药技术领域专题申请指南发布 (0/83) woody_681 2007-04-17 2007-04-17 22:20:22 by woody_681
    是否需要重新进行系统适用性验证?? (6/504) judy810809 2007-04-16 2007-04-17 21:46:03 by myqwyp
    [快捷药讯] 西药质量标准怎么做？？？？？？ (0/106) czj_1027 2007-04-17 2007-04-17 20:35:01 by czj_1027
    [快捷药讯] 如何得知某种新药进入哪期临床?? (5/385) lawyong_cpu 2007-04-14 2007-04-17 20:06:02 by lawyong_cpu
    [注册申报] 欧洲上市药物 (1/157) pengzhixia 2007-04-17 2007-04-17 16:18:29 by iamzane
    [政策法规] 求助：请教高手，中药提取物，要作为化药报，标准是否有变动？ (2/138) wrj112233 2007-04-16 2007-04-17 14:14:04 by wrj112233
    [资料求助] 求助 (0/160) yunxiang95 2007-04-17 2007-04-17 08:42:17 by yunxiang95
    [快捷药讯] 2007年头孢类药物预测    ( 1 2 ) (11/1043) hexuetao 2007-01-22 2007-04-16 21:25:34 by 天地之子
    [注册申报] 非处方药品申报及审核登记工作程序 (0/151) liljxl 2007-04-16 2007-04-16 19:00:31 by liljxl
    [快捷药讯] [原创]独发小木虫 药品批准文号普查现场核查 (2/222) 学员2Y76sI 2007-03-15 2007-04-16 17:44:47 by workyx
    请不吝赐教！关于溶媒残余的问题 (3/313) mosikaling 2007-01-05 2007-04-16 16:33:27 by sxw108868
    [质量控制] 包材取样，那位虫子知道呀，告我一声 (4/469) 又见白桦林 2007-03-06 2007-04-16 14:26:04 by 又见白桦林
    [资料求助] 维生素C单磷酸酯镁HPLC和UV的检测方法。 (0/68) doctorchen2000 2007-04-16 2007-04-16 13:36:34 by doctorchen2000
    [注册申报] COS注册申请表，还不知道的看看，应该没重复 (+3) (评阅+2) (金币≥50)(6/114) 木木木木 2006-06-09 2007-04-16 00:13:21 by longol
    [注册申报] OOS FDA guidance (+2) (评阅+2) (4/478) CZD1972 2006-07-16 2007-04-16 00:10:58 by longol
    [注册申报] 原料药COS注册QOS（Quality overall summary）电子模板    ( 1 2 ) (+8) (评阅+2) (金币≥50)(11/228) 木木木木 2006-06-07 2007-04-16 00:09:49 by longol
    [注册申报] 申请DMF EDMF COS提交审批程序的流程 (+2.75) (评阅+1) (6/601) crystalli 2006-06-03 2007-04-16 00:08:19 by longol
    [注册申报] DMF中文版    ( 1 2 ) (+6.5) (评阅+2) (14/817) beannail 2006-10-28 2007-04-16 00:04:06 by longol
    [质量控制] 哎！！看看被败倒的制药企业（被收回GMP证书）    ( 1 2 ) (13/1858) wangshouying 2007-03-12 2007-04-15 21:22:30 by ultrafrost
    资源 [ 查看全部 ] 作者 最后发表
    [关贴]研发中心管理制度 (7/332) hexinhua0920 2007-04-20 2007-04-21 22:28:35 by qcbnj
    [质量控制] [关贴]制药企业GMP (2/174) hexinhua0920 2007-04-21 2007-04-21 22:00:38 by yif2001
    [快捷药讯] [关贴]中药注射液质量标准汇总 (2/154) hexinhua0920 2007-04-21 2007-04-21 21:54:22 by yif2001
    [快捷药讯] [关贴]凝胶剂的处方与工艺 (1/236) hexinhua0920 2007-04-21 2007-04-21 21:34:17 by qla008
    [快捷药讯] [关贴]普利类药物合成 (4/163) movesky39 2007-04-07 2007-04-21 21:05:09 by cchh3969
    [质量控制] [关贴]QA部门操作标准 (1/129) hexinhua0920 2007-04-21 2007-04-21 17:52:57 by cpugoodboy
    [关贴]最新的乙醇国家标准 (1/151) hexinhua0920 2007-04-21 2007-04-21 17:49:09 by huigenghao
    [关贴]多靶点配体与药物设计( (1/84) hexinhua0920 2007-04-21 2007-04-21 17:48:56 by cpugoodboy
    [关贴]留样室管理制度及流程图 (3/296) hexinhua0920 2007-04-20 2007-04-21 16:40:20 by ling2386205
    [质量控制] [关贴]cGMP中文pdf版.rar (1/169) hexinhua0920 2007-04-21 2007-04-21 16:33:04 by ling2386205
    [质量控制] [关贴]某厂固体制剂全部操作标准 (0/192) hexinhua0920 2007-04-21 2007-04-21 09:04:34 by hexinhua0920
    [质量控制] 洁净室运行管理手册 (0/184) hexinhua0920 2007-04-21 2007-04-21 08:53:26 by hexinhua0920
    [质量控制] 生产线平衡的秘笈 (0/151) hexinhua0920 2007-04-21 2007-04-21 08:44:47 by hexinhua0920
    药品临床试验电子书 (15/1140) zh123456789 2006-11-26 2007-04-20 23:04:47 by forbbs
    [注册申报] 人用处方药和生物制品标签用法用量的内容和格式--FDA指南 (4/264) huigenghao 2007-04-14 2007-04-20 18:56:00 by 小小强
    [政策法规] 抗菌药物临床试验技术指导原则 (3/282) johnzhl01 2007-04-14 2007-04-20 18:53:52 by 小小强
    化学药品临床试验资料综述撰写格式与内容（DOC 29页）.rar (3/77) hexinhua0920 2007-04-18 2007-04-20 18:49:02 by 小小强
    [政策法规] 药物非临床研究质量管理规范认证管理办法 (1/151) lwjxz 2007-04-20 2007-04-20 17:32:27 by lwjxz
    [质量控制] [真情分享] “药品生产政策法规汇编” 07年最新版电子书! (2/145) irvin01056 2007-04-05 2007-04-20 12:19:26 by albance
    [质量控制] 水针设备 (5/259) 国枫521 2007-03-26 2007-04-20 12:07:11 by albance
    [注册申报] 最新COS编写培训教材 (14/305) 清风131 2007-03-24 2007-04-20 11:25:27 by lmyu1026
    我的收藏 (4/162) hexinhua0920 2007-04-19 2007-04-20 08:18:22 by cpugoodboy
    [质量控制] FDA工艺验证指南(中文） (4/492) maxuedong 2007-03-27 2007-04-19 20:35:41 by nauvet
    \临床试验方案样本.rar (1/180) hexinhua0920 2007-04-19 2007-04-19 20:10:25 by qla008
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    临床监查工作相关资料.rar (2/113) hexinhua0920 2007-04-19 2007-04-19 20:07:36 by qla008
    [质量控制] FDA对制药企业微生物实验室的检查指南 翻译稿 (16/938) xyzl 2007-03-07 2007-04-19 19:32:16 by hiwjp
    [政策法规] 推荐分享："药品包装、标签和说明书政策法规汇编"07.04.15 (0/118) irvin01056 2007-04-19 2007-04-19 14:08:31 by irvin01056
    [快捷药讯] 注射用炎琥宁冻干制剂全套申报资料.rar (0/159) hexinhua0920 2007-04-19 2007-04-19 14:03:28 by hexinhua0920
    嵇汝运院士的药学概论 (12/214) lfblessall 2007-04-14 2007-04-19 13:20:08 by johnzhl01
    [快捷药讯] 新药临床试验时间、费用及其他工作规划概要 (4/95) hexinhua0920 2007-04-18 2007-04-19 09:38:30 by englishood
    新药研发工作中的高效管理 (2/124) hexinhua0920 2007-04-18 2007-04-18 16:23:38 by qcbnj
    [注册申报] 药品注册现场核查工作方案！！！！ (3/244) hexinhua0920 2007-04-17 2007-04-18 09:54:52 by 小小强
    [关贴]呵呵，学习汇报停挂了（请理解）    ( 1 2 ) (73/1524) vipygm 2007-04-15 2007-04-17 23:25:23 by naoy
    [注册申报] 核查的几个关键点国家局给省局的解释 (32/2380) 小小强 2006-12-17 2007-04-17 21:36:22 by 清风131
    [政策法规] 化学药研究指导原则 (1/58) hexinhua0920 2007-04-17 2007-04-17 19:57:28 by samuel01
    [快捷药讯] 保健食品数据库 (4/361) cheng9gong 2006-12-16 2007-04-17 11:11:45 by dawed
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    [政策法规] 最新编辑“药品流通政策法规汇编” 电子书-无限制分享-！ (5/286) irvin01056 2007-03-15 2007-04-17 09:53:01 by irvin01056
    [注册申报] “药品注册政策法规汇编” 最新编辑电子书-无敌分享-带数据库检索哦！ (28/1418) irvin01056 2007-03-14 2007-04-17 09:48:37 by irvin01056
    [政策法规] [转]2005药典、国家药品标准和卫生部药品标准在线查询 (6/719) irvin01056 2007-04-13 2007-04-17 09:36:46 by irvin01056
    [注册申报] 2006年9月FDA新指导文件-quality system approach to pharmaceutical cGMP (8/452) yan1302 2006-12-01 2007-04-16 21:43:22 by xyzl
    [注册申报] 2007年药品注册安监工作会议交流材料 (6/203) johnzhl01 2007-04-14 2007-04-16 18:17:27 by 小小强
    [注册申报] 人用处方药和生物制品标签用法用量的内容和格式 (0/106) hqr1999 2007-04-16 2007-04-16 12:56:24 by hqr1999
    [注册申报] 新药审批流程 (1/215) iamzane 2007-04-15 2007-04-16 10:00:56 by 席夫碱
    [快捷药讯] 抗艾滋病药Efavirenz (依法韦伦)的合成 (8/762) Yu_G 2007-03-18 2007-04-15 22:03:39 by mililiuqiba
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