Helen J.
Regulatory Affairs consultant for medical device/ Quality system management
United States | America/Los_Angeles (USD)
$26/hr
Full-time : 30+ hrs/week
Full-time : 30+ hrs/week
0, Followers
ABOUT ME
Experienced Quality Assurance Consultant with a demonstrated history of working in Medical devices, Drugs, Biologics, and Combination products. Skilled in Regulatory Affairs, Quality Assurance, Clinical trials, New Drug Application (NDA), Investigational Drug Application (IND), Risk Assessment, Biologic License Application (BLA), and Consulting.