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- catalog contributor b2520269.
- catalog created "1989-1992.".
- catalog date "1989".
- catalog date "1989-1992.".
- catalog dateCopyrighted "1989-1992.".
- catalog description "Includes bibliographical references.".
- catalog description "v. 1. The Rules governing medicinal products for human use in the European Community -- v. 2. Notice to applicants for marketing authorizations for medicinal products for human use in the member states of the European Community -- v. 3. Guidelines on the quality, safety, and efficacy of medicinal products for human use. Addendum July 1990. Addendum May 1992 -- v. 4. Guide to good manufacturing practice for medicinal products -- v. 5. Veterinary medicinal products -- v. 6. Establishment by the European Community of maximum residue limits (MRLs) for residues of veterinary medicinal products in foodstuffs of animal origin.".
- catalog extent "6 v. in 8 :".
- catalog identifier "9282595633 (v. 1)".
- catalog issued "1989".
- catalog issued "1989-1992.".
- catalog language "eng".
- catalog publisher "Luxembourg : Office for Official Publications of the European Communities ; Washington, D.C. : European Community Information Service [distributor],".
- catalog spatial "Europe.".
- catalog spatial "European Economic Community countries.".
- catalog spatial "European Union countries.".
- catalog subject "344.4/04233 344.044233 20".
- catalog subject "Drug Industry standards Europe.".
- catalog subject "Drugs Law and legislation European Economic Community countries.".
- catalog subject "Drugs Law and legislation European Union countries.".
- catalog subject "European Economic Community.".
- catalog subject "KJE6191 .A42 1989".
- catalog subject "Legislation, Drug Europe.".
- catalog subject "Pharmaceutical Preparations standards Europe.".
- catalog subject "QV 33 GA1 R9 1989".
- catalog tableOfContents "v. 1. The Rules governing medicinal products for human use in the European Community -- v. 2. Notice to applicants for marketing authorizations for medicinal products for human use in the member states of the European Community -- v. 3. Guidelines on the quality, safety, and efficacy of medicinal products for human use. Addendum July 1990. Addendum May 1992 -- v. 4. Guide to good manufacturing practice for medicinal products -- v. 5. Veterinary medicinal products -- v. 6. Establishment by the European Community of maximum residue limits (MRLs) for residues of veterinary medicinal products in foodstuffs of animal origin.".
- catalog title "The Rules governing medicinal products in the European Community.".
- catalog type "text".