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2. [Changes in the norms governing practices for the manufacture of pharmaceutical products: implications for the MERCOSUR]. Temprano G, Prats S, Bregni C. Boll Chim Farm; 1998 Nov; 137(10):426-38. PubMed ID: 9880947 [Abstract] [Full Text] [Related]
6. WHO Expert Committee on Specifications for Pharmaceutical Preparations. World Health Organization. World Health Organ Tech Rep Ser; 2005 Nov; 929():1-142, backcover. PubMed ID: 16353684 [Abstract] [Full Text] [Related]
7. Merck: committed to access to medicines for patients throughout the world. Gilmartin RV. N J Med; 2000 Nov; 97(11):27-9. PubMed ID: 11103598 [No Abstract] [Full Text] [Related]
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14. Enforcement of the current good manufacturing practices for solid oral dosage forms after United States v. Barr Laboratories. Jimenez FA. Food Drug Law J; 1997 Sep; 52(1):67-82. PubMed ID: 10346711 [No Abstract] [Full Text] [Related]
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17. [Technicoscientific evolution and current direction of the standards regulating drug registration in Italy and in the European Economic Community]. Battaglino G. Boll Chim Farm; 1978 Jun; 117(6):313-24. PubMed ID: 743380 [No Abstract] [Full Text] [Related]
20. [Various aspects of the significance of government control in drug supply]. Teijgeler CA, Samsom RJ. Pharm Weekbl; 1969 Jun 27; 104(26):539-49. PubMed ID: 5788999 [No Abstract] [Full Text] [Related] Page: [Next] [New Search]