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2. I. Federal regulations concerning use of asbestos filters in manufacturing parenteral drugs. Casola AR Bull Parenter Drug Assoc; 1975; 29(5):216-8. PubMed ID: 1182330 [No Abstract] [Full Text] [Related]
3. Application of the Food and Drug Administration's current good manufacturing practices regulations to pharmacy practice: a legal view. Fink JL Contemp Pharm Pract; 1979; 2(4):202-5. PubMed ID: 10244540 [No Abstract] [Full Text] [Related]
4. The use of consultants in the parenteral industry. Agalloco JP J Parenter Sci Technol; 1986; 40(6):277-83. PubMed ID: 3819981 [No Abstract] [Full Text] [Related]
5. FDA regulations and guidelines. Rothschild A J Parenter Sci Technol; 1990; 44(1):26-9. PubMed ID: 2313489 [No Abstract] [Full Text] [Related]
6. When does compounding become manufacturing? Gushee J J Am Vet Med Assoc; 1994 Jul; 205(2):235-6. PubMed ID: 7928585 [No Abstract] [Full Text] [Related]
7. The parenteral drug industry: recent findings. Fry EM J Parenter Sci Technol; 1982; 36(2):55-8. PubMed ID: 7077464 [No Abstract] [Full Text] [Related]
8. II. Views of the pharmaceutical industry on the regulations. Newmark H Bull Parenter Drug Assoc; 1975; 29(5):218-21. PubMed ID: 1182331 [No Abstract] [Full Text] [Related]
9. Reaction of FDA to a fundamental change in the nature of regulations. Kennedy D J Parenter Drug Assoc; 1979; 33(1):17-20. PubMed ID: 253023 [No Abstract] [Full Text] [Related]
10. Separate manufacturing standards needed for veterinary drugs: AVMA. J Am Vet Med Assoc; 1996 Feb; 208(4):461. PubMed ID: 8603886 [No Abstract] [Full Text] [Related]
11. Drug development history, "overview," and what are GCPs? Heilman RD Qual Assur; 1995 Mar; 4(1):75-9. PubMed ID: 8520867 [TBL] [Abstract][Full Text] [Related]
12. Human and veterinary drugs: good manufacturing practices and proposed exemptions for certain OTC products. Fed Regist; 1978 Sep; 43(190 Pt 2):45013-89. PubMed ID: 10316700 [No Abstract] [Full Text] [Related]
13. Lessons learned from good manufacturing practice noncompliance. Peskoe MP Food Drug Law J; 1995; 50(1):65-70. PubMed ID: 10342986 [No Abstract] [Full Text] [Related]
14. Manufacturing misdeeds cost Abbott record-breaking payment. Lewis C FDA Consum; 2000; 34(3):38-9. PubMed ID: 11521253 [No Abstract] [Full Text] [Related]
15. Supplements and other changes to an approved application. Final rule. Food and Drug Administration, HHS Fed Regist; 2004 Apr; 69(68):18727-67. PubMed ID: 15072041 [TBL] [Abstract][Full Text] [Related]
16. 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; 52(1):67-82. PubMed ID: 10346711 [No Abstract] [Full Text] [Related]
17. Quality control and good manufacturing practices: safety and efficacy of commercial herbals. Awang DV Food Drug Law J; 1997; 52(3):341-4. PubMed ID: 10343036 [No Abstract] [Full Text] [Related]
18. Response to the applicability of proposed large volume parenteral regulations to small volume parenteral drug products. Bull Parenter Drug Assoc; 1976; 30(6):265-79. PubMed ID: 1000103 [No Abstract] [Full Text] [Related]
19. Application of good manufacturing practice regulations to investigational biologic products. Goebel PW J Parenter Drug Assoc; 1980; 34(5):348-51. PubMed ID: 6905865 [No Abstract] [Full Text] [Related]