M G de Jong
30 titels in de boekenbase · Auteur · Redacteur · 2003–2015
Educatieve uitgaven algemeenNaslagwerken algemeenNon-fictie informatief/professioneel algemeenEconomie en bedrijf algemeenManagement algemeen
Over M G de Jong
M G de Jong staat met 30 titels in de boekenbase als auteur en redacteur. Bekend van de series ‘CentER dissertation’ en ‘Clinical trial series’. Het werk valt vooral onder educatieve uitgaven algemeen, naslagwerken algemeen en non-fictie informatief/professioneel algemeen. Verschenen tussen 2003 en 2015 bij Erasmus Universiteit Research Institute of Management en Koninklijke Boom uitgevers PW.
Biovigilance
M G de Jong
Biovigilance
M G de Jong
Paperback · 2015
New survey methods
M.G. de Jong
New survey methods
M.G. de Jong
Paperback · 2013
Medical device clinical evaluation compliance guide
M.G. de Jong
Medical device clinical evaluation compliance guide
M.G. de Jong
Paperback · 2011
Medical Device Vigilance Compliance Guide
M.G. de Jong
Medical Device Vigilance Compliance Guide
M.G. de Jong
Paperback · 2011
Medical Device Clinical Evaluation Reference Guide
M G de Jong
Medical Device Clinical Evaluation Reference Guide
M G de Jong
Paperback · 2011
Medical device technical documentation reference guide
M.G. de Jong
Medical device technical documentation reference guide
M.G. de Jong
Paperback · 2011
Medical Device Clinical Trial Reference Guide
M.G. de Jong
Medical Device Clinical Trial Reference Guide
M.G. de Jong
Hardback · 2011
Medical Device Good Clinical Practice Reference Guide
M.G. de Jong
Medical Device Good Clinical Practice Reference Guide
M.G. de Jong
Hardback · 2011
Medical Device Vigilance Reference Guide
M.G. de Jong
Medical Device Vigilance Reference Guide
M.G. de Jong
Hardback · 2011
Good Clinical Practice Reference Guide for Medical Devices
M.G. de Jong
Good Clinical Practice Reference Guide for Medical Devices
M.G. de Jong
Hardback · 2011
Good clinical practices reference guide for medical device compliance
M.G. de Jong
Good clinical practices reference guide for medical device compliance
M.G. de Jong
Hardback · 2008
The future EU medical device regulatory system
M.G. de Jong
The future EU medical device regulatory system
M.G. de Jong
Hardback · 2007
The essentials of good regulatory compliance
H. Pieterse
The essentials of good regulatory compliance
H. Pieterse
Hardback · 2007
Medical Device Vigilance
M.G. de Jong
Medical Device Vigilance
M.G. de Jong
Hardback · 2007
Wegwijs in de Vennootschapsbelasting
J.N. Bouwman
Wegwijs in de Vennootschapsbelasting
J.N. Bouwman
Hardback · 2003
Open en besloten bij commanditaire vennootschappen en fondsen voor gemene rekening
M.G. de Jong
Open en besloten bij commanditaire vennootschappen en fondsen voor gemene rekening
M.G. de Jong
Paperback
Response Bias in International Marketing Research
M.G. de Jong
Response Bias in International Marketing Research
M.G. de Jong
Paperback
Clinical evaluation with medical devices
M.G. de Jong
Clinical evaluation with medical devices
M.G. de Jong
Hardback
State of the art clinical trials for medical devices
M.G. de Jong
State of the art clinical trials for medical devices
M.G. de Jong
Paperback
Medical device quality system compliance guide
M.G. de Jong
Medical device quality system compliance guide
M.G. de Jong
Paperback
Comparative Design Control Medicines and medical Devices
M.G. de Jong
Comparative Design Control Medicines and medical Devices
M.G. de Jong
Paperback
Informeer uw proefpersonen
M.G. de Jong
Informeer uw proefpersonen
M.G. de Jong
Losbladig
Inform your clinical research subjects
M.G. de Jong
Inform your clinical research subjects
M.G. de Jong
Losbladig
Practical medical device compliance
M.G. de Jong
Practical medical device compliance
M.G. de Jong
Practical medical device compliance
M.G. de Jong
Practical medical device compliance
M.G. de Jong
Niet gespecificeerd
Writing quality assurance procedures for clinical trials
M.G. de Jong
Writing quality assurance procedures for clinical trials
M.G. de Jong
Conducting clinical trials with medical devices
M.G. de Jong
Conducting clinical trials with medical devices
M.G. de Jong
Informed Consent Process
M.G. de Jong
Informed Consent Process
M.G. de Jong
Losbladig
A guide to European legislation directly and indirectly related to human Tissue Engineered Products
M.G. de Jong
A guide to European legislation directly and indirectly related to human Tissue Engineered Products
M.G. de Jong
Hardback
Designing medical devices
M.G. de Jong
Designing medical devices
M.G. de Jong
Paperback