357 related articles for article (PubMed ID: 19133627)
1. Validation and Six Sigma.
Barry E
Med Device Technol; 2008; 19(7):36, 38-40. PubMed ID: 19133627
[TBL] [Abstract][Full Text] [Related]
2. Meeting US and European supplier control requirements.
Donawa M
Med Device Technol; 2009; 20(3):24-7. PubMed ID: 19626952
[TBL] [Abstract][Full Text] [Related]
3. European requirements for product returns.
Donawa M
Med Device Technol; 2005 Nov; 16(9):28-31. PubMed ID: 16438446
[TBL] [Abstract][Full Text] [Related]
4. The impact of the revised electromagnetic compatibility standard.
Bozec D; Hayes DJ
Med Device Technol; 2004 Oct; 15(8):33-4, 36. PubMed ID: 16225272
[TBL] [Abstract][Full Text] [Related]
5. Implementing new European vigilance procedures.
Donawa M
Med Device Technol; 2007; 18(7):34, 36-7. PubMed ID: 18075133
[TBL] [Abstract][Full Text] [Related]
6. Preparing for more active market surveillance.
Donawa M
Med Device Technol; 2005 May; 16(4):30-3. PubMed ID: 15941197
[TBL] [Abstract][Full Text] [Related]
7. European medical device regulation: a new era?
Donawa M
Med Device Technol; 2004 Dec; 15(10):30-1. PubMed ID: 16225282
[TBL] [Abstract][Full Text] [Related]
8. Review of the Medical Device Directive.
Donawa M
Med Device Technol; 2003 Mar; 14(2):20-3. PubMed ID: 12698694
[TBL] [Abstract][Full Text] [Related]
9. The IVD directive: late-phase practicalities.
Johnson P; Walker R
Med Device Technol; 2003 Nov; 14(9):35-6. PubMed ID: 14682022
[No Abstract] [Full Text] [Related]
10. European Animal Tissue Directive.
Donawa M
Med Device Technol; 2004; 15(1):28-31. PubMed ID: 14994636
[TBL] [Abstract][Full Text] [Related]
11. How FDA-recognized standards impact users, manufacturers.
Osborn D
Biomed Instrum Technol; 2009; 43(2):156-7. PubMed ID: 19480488
[No Abstract] [Full Text] [Related]
12. Final FDA inspection manual.
Donawa M
Med Device Technol; 2001 Apr; 12(3):29-32. PubMed ID: 11547684
[TBL] [Abstract][Full Text] [Related]
13. FDA pilot programme in support of global harmonisation.
Donawa ME
Med Device Technol; 2003 Nov; 14(9):32-4. PubMed ID: 14682021
[TBL] [Abstract][Full Text] [Related]
14. Medical devices on trial, Part I.
Wright D
Med Device Technol; 2002 Dec; 13(10):35-8. PubMed ID: 12575529
[TBL] [Abstract][Full Text] [Related]
15. Process validation: harmonizing the requirements.
Donawa ME
Med Device Technol; 1998 Oct; 9(8):13-6. PubMed ID: 10186986
[TBL] [Abstract][Full Text] [Related]
16. A new year's revelation: the boss needs training too.
Donawa ME
Med Device Technol; 1995; 6(1):11-3. PubMed ID: 10155369
[TBL] [Abstract][Full Text] [Related]
17. Clinical evaluations clinical investigations under the amended Medical Device Directive.
Dannhorn DR; Schwabedissen H
Med Device Technol; 2008 Sep; 19(5):16-8, 20. PubMed ID: 18947145
[TBL] [Abstract][Full Text] [Related]
18. Conducting clinical studies in Italy.
Donawa M
Med Device Technol; 2005 Oct; 16(8):21-4. PubMed ID: 16355966
[TBL] [Abstract][Full Text] [Related]
19. IVD authorized representatives.
Donawa ME
Med Device Technol; 2003 May; 14(4):19-21. PubMed ID: 12774572
[TBL] [Abstract][Full Text] [Related]
20. Validation.
Isaacs A
Med Device Technol; 2001 Dec; 12(10):38, 40. PubMed ID: 15966146
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
