I started out as a test technician for a medical device company and my career in the industry evolved from there, working in research & development, quality, and now in the regulatory field!

Since joining MIP, I’ve grown a passion for FDA strategy and submissions. Learning from Kwame as an industry leader has been incredibly rewarding. His expertise has given me valuable insights into regulatory affairs, clinical trials, market access, and reimbursement. This knowledge has helped me grow in the field rapidly! I’ve learned to better serve our clients by aligning regulatory decisions with their broader business objectives.

I am looking forward to  gaining my Regulatory Affairs Certification (RAC) this year. This will deepen my knowledge of device regulatory affairs and expand my skills, allowing me to contribute more effectively and position myself for future career advancements with MIP!