Essentials of Good Regulatory Compliance
English, 14 pages
€ 15.00
Medical Device Vigilance
English, 51 pages
€ 35.00
The Vision for a Future EU Medical Device Regulatory System
Information technology developments, globalisation of business and global harmonisation of medical device
requirements will mean that the EU regulatory system will have to simplify and consolidate if it is to ensure EU
can meet competitive and business objectives of the EU is the vision of the authors. Written by H Pieterse and
M G de Jong.
English, 11 pages
€ 25.00
Proper clinical development of medical devices to ensure continuity of care
Proper clinical development of medical devices to ensure continuity of care is verschenen in Edition 8 van Health Information Developments in the Netherlands. 2006. Written by Herman Pieterse and Marja de Jong, pages 51-55.
English, 4 pages
€ 25.00
The essentials of Good Regulatory Compliance
Regulatory Affairs Journal Vol 14, No 5 Sept/Oct 2006, page 293-298.
English, 5 pages
€ 25.00
Een degelijke klinische ontwikkeling van medische hulpmiddelen
Een degelijke klinische ontwikkeling van medische hulpmiddelen is een vereiste om de continuïteit van zorg te garanderen.
H. Pieterse en M.G. de Jong.
NTMA September 2006, 10-17
Dutch, 7 pages
€ 25.00
Proper clinical development of medical devices to ensure continuity of care
H. Pieterse and M.G. de Jong, Health information developments in the Netherlands, Edition 8, 2006, 51-56.
English, 5 pages
€ 25.00
Changes Affecting the Clinical Evaluation of Medical Devices
The Regulatory Affairs Journal (Devices) Vol 13 No 6 Nov/Dec 2005 355-362
English, 8 pages
€ 25.00
The future of computerization at the investigator site
Herman Pieterse April 1998.
Health Information Initiatives in the Netherlands [et al.; ed. W. Dekker] Amsterdam, The Dutch Association for Medical Records Administration.
A. Hasman, Professor. With literature references ISBN 90-802225-4-2.
English, 8 pages
€ 8.00