Dear ISO 13485 Team, specially to Roland CE 0120
When I implement ISO 13485, there are problem about:
1:-Advisory notice,
2:-Early warning,
3:-Product recall,
4: Adverst event,
5:-Post production phase,
If you have practically conduct, you advice is appliciate,
:confused:
DRDDO

Can you be more specific about what information you want? What are the specific problems you have?