RICHARD JANOSKO CONSULTING

Updated 160 days ago
  • ID: 7213442/143
I am an experienced Medical Device Regulatory Affairs Consultant. I understand the engineering, manufacturing, marketing and regulatory needs of both large and small medical device manufacturing organizations. My background is rooted in medical device engineering and development. I have over thirtyfive years experience in medical device companies from hands-on engineering, to top level Development Engineering and Regulatory Affairs management for United States, European and Asian companies... My FDA and ISO medical device regulatory affairs background includes positions as the domestic and International Regulatory Affairs Director for Siemens Ultrasound Division and Siemens Oncology Care Group, as well as Regulatory Affairs Consultant to medical device companies in the United States, Canada, Asia, and Europe... Richard Janosko Certified FDA Medical Device Regulatory Affairs Consulting, Premarket Notification 510(k) preparation, GMP procedures, and audits, Form 483, warning letter,..
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Interest Score
2
HIT Score
0.00
Domain
janosko.com

Actual
www.janosko.com

IP
209.204.140.109

Status
OK

Category
Company
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