The method of clinical investigation for active implantable medical devices are described in article 8 of the Royal Decree dated 15/07/1997 (French version) amended by the Royal Decree dated 10/12/2002 (French version) and by the Royal Decree dated 21/01/2009 (French version) (+1 appendix) relating to medical devices (converting the European directive 90/385 ) and those concerning the other medical devices in article 9 of the Royal Decree dated 18/03/1999 (French version) converting the European directive 93/42.
Information about the clinical investigations is available in the following sections:
- AIMD (information in Dutch) - (information in French)
- IVD (information in Dutch) - (information in French)
Federal Agency for Medicines and Health Products
Place Victor Horta, 40 box 40
Email : email@example.com