Regulatory requirements for dental materials/equipment
Legislation, standardisation and quality
Medical devices in the European market: highlights of the new medical device regulation (MDR). The importance of standardisation on the quality of dental materials will be discussed. How can the dentist and the patient ensure safe materials?
- Legislation
- Standardisation
- Quality
This course is accepted in the continuing education program for the Norwegian Dental Association (NDA/NTF).
Duration:
The lecture can be held as a 30 min presentation or as an extended version lasting up to 1,5 hours.
Contact:
Please contact us if you want to more information about content, cost or our time schedule. We look forward to hearing from you!
Lecturer:
Hilde M. Kopperud,
Head of laboratory,
Dr. scient
Hilde is responsible for NIOMs accredited test laboratory for the evaluation of biomaterials according to requirements in ISO-standards. She is also an expert in the EU-expert panel for medical devices according to MDR. She has been working with international and European standardization since 2003, as a convener and expert in several working groups in ISO TC 106 Dentistry.