“Medical devices range from simple tongue depressors and bedpans to complex programmable pacemakers with micro-chip technology and laser surgical devices.” - FDA
Is your organization ready for the 2020 Medical Device Regulation compliance in the EU?
Have you established and maintained structure around your Clinical Evaluation Report (CER)?
Does your team require training for MDR requirements and maintenance?
Do you need an overall gap analysis of your system to identify the strengths and weaknesses of your current system?
Do you need help with COFEPRIS registration in Mexico?
We at Metis Consulting Services can help.
Call us at (760) 443-2659 to learn more, or send us an email at info@ metisconsultingservices.com
Last updated: 9 October 2019