Grishma Mistry
Regulatory Consultant
Since completing my internship at Advena and obtaining a MEng in Biomedical Engineering in 2020, I
have gained over 3 years of experience within Medical Device Regulatory Affairs. I am experienced in
the creation of Technical Documentation that is compliant with EU MDD, EU MDR and UK MDR
2002, including the creation of Clinical Evaluation Plans and Reports, Biological Assessment Reports
and Post Market Surveillance.