医药海外商情与Dialog课件1

单击此处编辑母版标题样式,单击此处编辑母版文本样式,第二级,第三级,第四级,第五级,0,30 十一月 2024,1,医药海外商情与Dialog(1),海外市场,(,产品,),信息,全球公司名录,化工企业信息药物公司名录新药公布信息,其他,Dialog,能提供哪几方面信息,海外公司信息,市场调研报告证券分析报告,海关贸易统计产品新闻动态其他,法律、法规信息,海外公司名录,全球公司名录,Kompass,系列,数据库（找寻贸易伙伴）,提供全球近,200,万家企业（美国,50,000,、加拿大,8,000,、西欧,970,000,、东欧,348,000,、亚太,214,000,、非洲中东,137,000,、拉美,14,600,）的详细资料，包括公司地址、电话、传真等联系方式、公司员工数、主要产品，公司动态、总经理等高层人员姓名等。,Kompass Asia/Pacific,Kompass Canada,Kompass Central/Eastern Europe,Kompass Latin America,Kompass Middle East/Africa/Mediterranean,Kompass USA,Kompass Western Europe,http:/ materials for pharmaceuticals(trade),海外公司信息,化学公司名录,Directory of Chemical Producers-Companies,数据库,produced by SRI Consulting,a division of Access Intelligence LLC,is a database of international manufacturers of commercial chemical products.Data correspond to the companies section of SRI Consultings printed Directory of Chemical Producers(DCP)withthe important advantage of full multi-region searchability.,查找,Simvastatin,国外生产厂商？,海外公司信息,药物公司名录,IMS Company Search,数据库,IMS Company Search profiles the most significant pharmaceutical companies,including subsidiaries of multinationals,operating within the worlds main health care markets.The database covers over 7 thousand pharmaceutical organizations in more than 60 countries.Details provided include name,address,e-mail and Web sites together with IMS Health MIDAS sales data and more than 7,700 senior executives names.,查找,AKZO NOBEL,的公司的许可状况,海外公司信息,药物公司信息,IMS Company Profiles,数据库,Examines annually the internal make-up of 110 key pharmaceutical companies worldwide.Each individual profile analyzes the critical components that affect a companys business strategy,giving a clear assessment of a companys relative strengths and weaknesses.Companies profiled range from large to small,public and private,and produce ethical,biotech,and generic pharmaceuticals.,掌握,ABBOT,公司全方位信息,(,药品研发图,财务,产品,市场展望,.,),海外公司信息,新药发布信息,IMS New Product Focus,制剂上市信息数据库,IMS New Product Focus monitors launches of new ethical pharmaceutical product introductions internationally,providing invaluable competitor information on new drug launches.,跟踪,simvastatin,在全球的上市,海外市场,(,产品,),信息,产品新闻动态,Newsroom,数据库,Dialog NewsRoom,全球新闻信息服务的信息来源高达,11,000,多个，包括来自全球重点商业和贸易期刊的，地方的、地区的和国际的知名的报纸和杂志，公司新闻发布、广播稿和行业内部通讯等等。事实上，每个行业都已涵盖，从银行业到生物技术，从生活消费品到化工。另外，,Dialog NewsRoom,还提供回溯,30,年的深度历史存档，根据以往事件和趋势提供有助益分析和前景预测,Dialog(File 990)Current,Dialog(File 991)2005 Archive,Dialog(File 992)2004 Archive,Dialog(File 993)2003 Archive,Dialog(File 994)2002 Archive,Dialog(File 995)2001 Archive,海外市场,(,产品,),信息,产品新闻动态,Newsroom,数据库,Dialog NewsRoom,所包含的医药杂志资源,(,部分,),海外市场,(,产品,),信息,产品新闻动态,Newsroom,数据库,Dialog NewsRoom,所包含的医药杂志资源,(,部分,),海外市场,(,产品,),信息,海外市场,(,产品,),信息,Tablebase,该数据库主要提供公司，产品，产业，品牌，市场，等等世界范围内表格式信息。所有的记录都有一张表格和可得到的原记录)。表格数据是该数据库的主旋律，每份表格都有清晰明了的标题。每周更新。,海外市场,(,产品,),信息,海关贸易统计,Tradstat,汇聚,40,个国家的海关进出口数据,涵盖,90%,以上世界贸易活动,Dialogtradstat,是记录世界各国海关进出口数据的统计系统，支持5种报告格式，通过,Tradstat,系统可以轻松了解各个国家进口产品的数量和金额。,海外市场,(,产品,),信息,Dialog Tradstat,可以提供五种报告类,型,I,mports/Exports,Reports,进口,/,出口报告,显示某一目标国家及其世界各地的贸易伙伴之间进出口,个别产品或同类产品的贸易信息,K,ey Countries Report,主要国家报告,在一个报告中整合所有“,TradStat,报告国家”,即指,Tradstat,提供原始贸易数据的国家，以显示个别产品或同,产品的进出口信息,R,egion Reports(EU),区域报告（欧,盟,）,报告整合了欧盟成员国的进出口贸易信息，并显示欧盟,为一贸易单位跟世界各国的贸易统计数据,S,ector Breakdown,Reports,行业细分报告,显示某一市场部分的细分报告，提供某一行业的概述以,该行业具体产品的详细贸易信息,Trend Reports,贸易趋势报告,显示某一目标国家及其世界各地的贸易伙伴之间个别产,或者同类产品的贸易信息，您可以一目了然地识别贸易,进口或出口变化趋势,海外市场,(,产品,),信息,市场调研报告,Market Research,Covers over 700 Industries,250,000,Reports,170,Publishers,海外市场,(,产品,),信息,市场调研报告,Market Research,Market,Research,海外市场,(,产品,),信息,市场调研报告,Market Research,Market,Research,海外市场,(,产品,),信息,市场调研报告,Market Research,海外市场,(,产品,),信息,海外市场,(,产品,),信息,海外市场,(,产品,),信息,证券分析报告,Broker Research,贸易活动,由二百多万份证券商报告、经济研究报告组成，涉及世界各地超过37，500家公司。这些报告来自世界各地超过650家投资银行、经济事务所以及咨询公司未经改动的报告。另外还包括大量的分析师晨会纪录，为战略规划提供有力支持,法律、法规及其他,DIOGENES?/sup:Adverse Drug Events Database consists of two subfiles:Adverse Drug Reactions(ADR)and Adverse Event Reporting System(AERS).ADR records contain data regarding a single patients experience with a drug or combination of drugs as reported to the U.S.Food and Drug Administration(FDA).Since 1969,the FDA has legally-mandated adverse drug reaction reports from pharmaceutical manufacturers and maintained them in their ADR system.The original reports varied greatly in detail,some providing only minimal details.,In November 1997,the ADR database was replaced by the Adverse Event Reporting System(AERS).AERS events are described on MedWatch form DGA-3500A and contain many more details than appeared on the earlier ADR records.Reports in the AERS file are evaluated by clinical reviewers in FDAs Center for Drug Evaluation.When information is unknown,it is omitted.,Vaccines are reported in a separate system and are not included in ADR data.,法律、法规及其他,法律、法规及其他,FDAnews,provides domestic and international regulatory,legislative,and business news and information for executives in industries regulated by the U.S.Food and Drug Administration and The European Commission.,Th