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89/381/EWG*89/381/EEC*89/381/CEE

Council directive of 14 June 1989 extending the scope of directives 65/65/EEC and 75/319/EEC on the approximation of provisions laid down by law, regulation or administrative action relating to proprietary medicinal products and laying down special provisions for medicinal products derived from human blood or human plasma (89/381/EEC)

Số trang: 3
Ngày phát hành: 1989-06-14

Liên hệ
Số hiệu tiêu chuẩn
89/381/EWG*89/381/EEC*89/381/CEE
Tên tiêu chuẩn
Council directive of 14 June 1989 extending the scope of directives 65/65/EEC and 75/319/EEC on the approximation of provisions laid down by law, regulation or administrative action relating to proprietary medicinal products and laying down special provisions for medicinal products derived from human blood or human plasma (89/381/EEC)
Ngày phát hành
1989-06-14
Trạng thái
Hết hiệu lực
Tiêu chuẩn tương đương
Tiêu chuẩn liên quan
Thay thế cho
Thay thế bằng
2001/83/EG*2001/83/EC*2001/83/CE (2001-11-06)
Directive 2001/83/EC of the European Parliament and of the Council of 6 November 2001 on the Community code relating to medicinal products for human use
Số hiệu tiêu chuẩn 2001/83/EG*2001/83/EC*2001/83/CE
Ngày phát hành 2001-11-06
Mục phân loại 11.120.10. Thuốc
Trạng thái Có hiệu lực
Lịch sử ban hành
89/381/EWG*89/381/EEC*89/381/CEE (1989-06-14)
Council directive of 14 June 1989 extending the scope of directives 65/65/EEC and 75/319/EEC on the approximation of provisions laid down by law, regulation or administrative action relating to proprietary medicinal products and laying down special provisions for medicinal products derived from human blood or human plasma (89/381/EEC)
Số hiệu tiêu chuẩn 89/381/EWG*89/381/EEC*89/381/CEE
Ngày phát hành 1989-06-14
Mục phân loại 11.120.10. Thuốc
Trạng thái Có hiệu lực
* 2001/83/EG*2001/83/EC*2001/83/CE (2001-11-06)
Directive 2001/83/EC of the European Parliament and of the Council of 6 November 2001 on the Community code relating to medicinal products for human use
Số hiệu tiêu chuẩn 2001/83/EG*2001/83/EC*2001/83/CE
Ngày phát hành 2001-11-06
Mục phân loại 11.120.10. Thuốc
Trạng thái Có hiệu lực
Từ khóa
Analysis * Biotechnology * Blood * Blood plasma * Chemical analysis and testing * Chemical hazards * Dangerous materials * Drugs * Health services * Laboratories * Marking * Pharmacy * Production * Specification (approval) * Surveillance (approval) * Toxic materials * Checks * Testing * Chemicals * Medicine * Medicaments * European Communities
Mục phân loại
Số trang
3