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现行 EEC 83/570/EEC
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Proprietary Medicinal Products amending 65/65/EEC 修订65/65/EEC的专利药品
发布日期: 1983-10-26
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发布单位或类别: 未知国家-其他未分类
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现行
EEC 66/454/EEC
Proprietary Medicinal Products - Amending 65/65/EEC
专利药品-修订65/65/EEC
1966-01-01
现行
EEC 87/21/EEC
Proprietary Medicinal Products Amending 65/65/EEC
修订65/65/EEC的专利药品
1987-01-01
现行
EEC 89/341/EEC
Proprietary Medicinal Products Amending 65/65/EEC
修订65/65/EEC的专利药品
1989-05-03
现行
EEC 93/39/EEC
Medicinal Product Directive - Included in volume 65/65/EEC
药品指令-包含在第65/65/EEC卷中
1993-01-01
现行
EEC 93/2309/EEC
Medicinal Products - Evaluating Agencies - Included in volume 65/65/EEC
药品.评估机构.包括在第65/65/EEC卷中
1993-01-01
现行
EEC 75/319/EEC
Medicinal Products Directive - Also included in volume 65/65/EEC Complete
医药产品指令——也包含在第65/65/EEC卷中
1975-01-01
现行
EEC 89/341 Cor 1
Corrigendum to Council Directive 89/341/EEC of 3 May 1989 Amending Directives 65/65/EEC, 75/318/EEC and 75/319/EEC on the Approximation of Provisions Laid Down by Law, Regulation or Administrative Action Relating to Proprietary Medicinal Products
1989年5月3日修订指令65/65/EEC、75/318/EEC和75/319/EEC的理事会指令89/341/EEC的勘误表 该指令与专利药品相关的法律、法规或行政行为所规定的条款近似
1989-06-23
现行
MEDDEV 2.1/3
Guidelines Relating to the Demarcation Between 90/385/EEC on Active Implatable Medical Devices, 93/42/EEC on Medical Devices,65/65/EEC Relating to Medicinal Products & Related Directives
关于90/385/EEC(关于有源可植入医疗设备)、93/42/EEC(关于医疗设备)、65/65/EEC(关于医疗产品和相关指令)之间划分的指南
1998-03-01
现行
EEC 65/65/EEC
Council Directive 65/65/EEC of 26 January 1965 on the approximation of provisions laid down by law, regulation or administrative action relating to medicinal products
1965年1月26日关于与医药产品有关的法律、法规或行政行为规定的近似性的委员会指令65/65/EEC
1965-01-26
现行
EEC 91/507/EEC
Council Directive 91/507/EEC of 22 December 1986 Amending Directive 75/318/EEC on the Approximation of the Laws of the Member States Relating to Analytical, Pharmaco-Toxicological and Clinical Standards and Protocols in Respect of the Testing of Proprietary Medicinal Products
1986年12月22日的理事会指令91/507/EEC修订了关于 成员国有关专利药品测试的分析、药物毒理学和临床标准及协议的法律近似值
1991-07-19
现行
EEC 87/19/EEC
Council Directive 87/19/EEC of 22 December 1986 Amending Directive 75/318/EEC on the Approximation of the Laws of the Member States Relating to Analytical, Pharmaco-Toxicological and Clinical Standards and Protocols in Respect of the Testing of Proprietary Medicinal Products
1986年12月22日的理事会指令87/19/EEC修订了关于 成员国有关专利药品测试的分析、药物毒理学和临床标准及协议的法律近似值
1986-12-22
现行
EEC 1987/15
Council Directive of 22 December 1986 Amending Directive 75/318/EEC on the Approximation of the Laws of the Member States Relating to Analytical, Pharmaco-Toxicological and Clinical Standards and Protocols in Respect of the Testing of Proprietary Medicinal Products
1986年12月22日修订75/318/EEC号指令的理事会指令 该指令与成员国有关专利药品测试的分析、药物毒理学和临床标准及协议的法律近似
1987-01-17