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Good clinical practices in (nuclear) research
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Guidance for the regulatory status of allergen extracts in clinical trials
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- Journal Article
- A2
- open access
Good clinical practice in clinical interventional studies
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Regulatory-clinical methodologies for medical device clincal trials
(2008) -
The future of the EU Medical Device Regulatory System: globalisation, simplification, centralisation and automation.
(2007) -
State of the art clinical trials for medical devices: a guide to Good Clinical Practices compliance.
(2007) -
Essentials of Good Regulatory Compliance: the REACT principles.
(2007) -
A vision for Eu Device Regulation.
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Is the Migraid (R) device an asset in the non-pharmacologic treatment of migraine?
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Een degelijke klinische ontwikkeling van medische hulpmiddelen is een vereiste om de continuïteit van zorg te garanderen.
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Proper clinical development of medical devices to ensure continuity of care.
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The essentials of Good Regulatory Compliance.
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The changing regulatory environment for the clinical evaluation of medical devices in Europe.
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Instruction manual for the conduct of clinical research with medicinal products in the Netherlands: a practical guide for the design, preparation, conduct and reporting.
(2004) -
Richtsnoer voor Good Clinical Practice (CPMP/ICH/135/95).
(2004)