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Regulatory-clinical methodologies for medical device clincal trials

Herman Pieterse (UGent)
(2008)
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Citation

Please use this url to cite or link to this publication:

MLA
Pieterse, Herman. “Regulatory-clinical Methodologies for Medical Device Clincal Trials.” 2008 : n. pag. Print.
APA
Pieterse, H. (2008). Regulatory-clinical methodologies for medical device clincal trials. Ghent University. Faculty of Medecine and Health Sciencs ; Profess Medical Consultancy, Ghent, Belgium ; Heerhugowaard, The Netherlands.
Chicago author-date
Pieterse, Herman. 2008. “Regulatory-clinical Methodologies for Medical Device Clincal Trials”. Ghent, Belgium ; Heerhugowaard, The Netherlands: Ghent University. Faculty of Medecine and Health Sciencs ; Profess Medical Consultancy.
Chicago author-date (all authors)
Pieterse, Herman. 2008. “Regulatory-clinical Methodologies for Medical Device Clincal Trials”. Ghent, Belgium ; Heerhugowaard, The Netherlands: Ghent University. Faculty of Medecine and Health Sciencs ; Profess Medical Consultancy.
Vancouver
1.
Pieterse H. Regulatory-clinical methodologies for medical device clincal trials. [Ghent, Belgium ; Heerhugowaard, The Netherlands]: Ghent University. Faculty of Medecine and Health Sciencs ; Profess Medical Consultancy; 2008.
IEEE
[1]
H. Pieterse, “Regulatory-clinical methodologies for medical device clincal trials,” Ghent University. Faculty of Medecine and Health Sciencs ; Profess Medical Consultancy, Ghent, Belgium ; Heerhugowaard, The Netherlands, 2008.
@phdthesis{6916355,
  author       = {Pieterse, Herman},
  isbn         = {9789080477186},
  language     = {eng},
  pages        = {176},
  publisher    = {Ghent University. Faculty of Medecine and Health Sciencs ; Profess Medical Consultancy},
  school       = {Ghent University},
  title        = {Regulatory-clinical methodologies for medical device clincal trials},
  year         = {2008},
}