108 related articles for article (PubMed ID: 15859135)
1. [Clinical trial of medical device and new GCP].
Ishimaru S
Nihon Geka Gakkai Zasshi; 2005 Apr; 106(4):273. PubMed ID: 15859135
[No Abstract] [Full Text] [Related]
2. An outline for public registration of clinical trials evaluating medical devices.
Popp RL; Lorell BH; Stone GW; Laskey W; Smith JJ; Kaplan AV
J Am Coll Cardiol; 2006 Apr; 47(8):1518-21. PubMed ID: 16630985
[TBL] [Abstract][Full Text] [Related]
3. When to conduct a clinical trial.
Boutrand JP
Med Device Technol; 2004 Oct; 15(8):28-31. PubMed ID: 16225271
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. Statistical and regulatory issues in nonrandomized medical device clinical studies.
Li H; Yue LQ
J Biopharm Stat; 2008; 18(1):20-30. PubMed ID: 18161539
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. Risk management of European device clinical studies.
Donawa M
Med Device Technol; 2007; 18(2):39-42. PubMed ID: 17494500
[TBL] [Abstract][Full Text] [Related]
8. Experience with reviewing Bayesian medical device trials.
Pennello G; Thompson L
J Biopharm Stat; 2008; 18(1):81-115. PubMed ID: 18161543
[TBL] [Abstract][Full Text] [Related]
9. Performance evaluation and the IVD Directive.
Spencer S
Med Device Technol; 2002 Nov; 13(9):41-3. PubMed ID: 12534158
[TBL] [Abstract][Full Text] [Related]
10. Successful recruitment for medical device clinical studies.
Donawa M
Med Device Technol; 2004 Oct; 15(8):25-7. PubMed ID: 16225270
[TBL] [Abstract][Full Text] [Related]
11. [How to assess new medical devices].
Bernard A; Vicaut E
J Chir (Paris); 2009 Apr; 146(2):129-35. PubMed ID: 19524920
[TBL] [Abstract][Full Text] [Related]
12. Conducting clinical studies in Italy.
Donawa M
Med Device Technol; 2005 Oct; 16(8):21-4. PubMed ID: 16355966
[TBL] [Abstract][Full Text] [Related]
13. Update on the forthcoming European Clinical Investigation Standards.
Donawa M
Med Device Technol; 2002 Sep; 13(7):24-5. PubMed ID: 12397830
[TBL] [Abstract][Full Text] [Related]
14. Clinical investigation of medical devices.
Stewart RR
Med Device Technol; 1995 Jun; 6(5):36-40. PubMed ID: 10155392
[TBL] [Abstract][Full Text] [Related]
15. Managing clinical data for worldwide acceptance.
Donawa M
Med Device Technol; 2006 Oct; 17(8):26-8. PubMed ID: 17153369
[TBL] [Abstract][Full Text] [Related]
16. Group makes recommendations to speed FDA device approvals.
Scott L
Mod Healthc; 1993 May; 23(19):23. PubMed ID: 10125877
[No Abstract] [Full Text] [Related]
17. German law: the differences.
Müller-Lierheim WG
Med Device Technol; 1997 Nov; 8(9):38-40. PubMed ID: 10174630
[TBL] [Abstract][Full Text] [Related]
18. Proposed amendments to the medical devices Directives.
Donawa M
Med Device Technol; 2006; 17(1):22-5. PubMed ID: 16483107
[TBL] [Abstract][Full Text] [Related]
19. Clinical research and the development of new devices: considerations for nurses.
Lanter J
Dimens Crit Care Nurs; 2007; 26(3):117-20. PubMed ID: 17440296
[TBL] [Abstract][Full Text] [Related]
20. [Differences between clinical trials according to the German law on pharmaceuticals (Arzneimittelgesetz) and trials according to the German law on medical products (Medizinproduktegesetz)].
Krummenauer F
Ophthalmologe; 2003 Feb; 100(2):150-4. PubMed ID: 12589461
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]