THE NEW ISO 14155 REQUIREMENTS FOR MEDICAL DEVICE CLINICAL STUDIES 2011 is a conference that covers topics such as:
- The ISO 14155 Standard and medical device studies
- Changes in the ISO 14155 Standard
- Study documentation and adverse event reporting
- Updating the company`s standard operating procedures and quality system according to ISO 14155 changes
- Ideas and Tips for updating the company`s systems in order to comply withthe standard
THE NEW ISO 14155 REQUIREMENTS FOR MEDICAL DEVICE CLINICAL STUDIES brings together Anyone who is involved in conducting medical device studies including regulatory, clinical, research and quality staff involved in medical device clinical investigations and post market surveillance studies.
