After completing her Internship at Advena, Grishma obtained an MEng in Biomedical Engineering. She continues to support the Consultancy team gaining particular experience in the creation, development and completion of Clinical Evaluation Reports to MEDDEV 2.7.1 rev 4 and Biological Evaluation Assessments to the requirements of EN ISO 10993.
Sarah Pavitt
Senior Regulatory & Quality Consultant
A senior Consultant with over 9 years in medical devices industry working on airways, COPD, IVF and ventilator devices. Responsible…
Andrea Meikle
Business Administrator (UK)
Andrea joined the UK Admin Team as an experienced Business Administrator/Office Manager; mainly in Higher Education. Her focus now is…
Leeanne Baker
Regulatory Consultant
A Medical Device consultant with extensive experience of both regulatory and quality projects in accordance with both European and United…