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3. How to handle a product problem. Harris PC MLO Med Lab Obs; 1985 Sep; 17(9):61-70. PubMed ID: 10317744 [No Abstract] [Full Text] [Related]
4. Medical device and laboratory product problem reporting program (PRP). FDA Drug Bull; 1979 Nov; 9(5):30. PubMed ID: 510843 [No Abstract] [Full Text] [Related]
5. Hospitals wary of interpretation of medical device reporting law. Burke M Hospitals; 1991 Oct; 65(20):40, 42. PubMed ID: 1916713 [No Abstract] [Full Text] [Related]
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11. Safe Medical Devices Act of 1990: current hospital requirements and recommended actions. Alder H Healthc Facil Manag Ser; 1993 Sep; ():1-34. PubMed ID: 10132639 [TBL] [Abstract][Full Text] [Related]
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13. CLR 1994-1995. Product information section. MLO Med Lab Obs; 1994; Suppl():11-155. PubMed ID: 10171912 [No Abstract] [Full Text] [Related]
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15. MedWatch: the new medical products reporting program. Couig MP; Merkatz RB Am J Nurs; 1993 Aug; 93(8):65-8. PubMed ID: 8256839 [No Abstract] [Full Text] [Related]
16. Who will regulate devices? Nurses and hospitals. Lewis HL Mod Hosp; 1973 Nov; 121(5):74-6. PubMed ID: 4786790 [No Abstract] [Full Text] [Related]
17. Food and Drug Administration--General hospital and personal use devices; general provisions. Final rule. Fed Regist; 1980 Oct; 45(205):69678-737. PubMed ID: 10248451 [TBL] [Abstract][Full Text] [Related]
18. What is the Medical Device and Lab Product Problem Reporting Program? Moore R Pharm Times; 1982 Nov; 48(11):53-7. PubMed ID: 10257641 [No Abstract] [Full Text] [Related]
19. Medical device legislation. Miller MJ Hospitals; 1973 Jun; 47(11):81-8. PubMed ID: 4706560 [No Abstract] [Full Text] [Related]
20. A "complaint department" for medical devices. Thompson RC FDA Consum; 1987 Mar; 21(2):10-3. PubMed ID: 10312180 [No Abstract] [Full Text] [Related] [Next] [New Search]