Ananthi Subash
Member since: Jan 21, 2019
Published articles: 1
Medical Device Risk Analysis
Risk management is one of the essential process having greater importance for CE marking of a medical device to be sold in the European market. CE certification is mandatory. To obtain CE marking...
Articles > Writing > Self Publishing
Feb 18, 2019
Author Bio
Myself Dr. Ananthi Subash MSc., Ph.D in Biotechnology. Currently specialized in Medical Device Regulatory requirements for US FDA and EU Regulation by involving in Biological Evaluation, Risk Analysis and Clinical Evaluation at I 3 CONSULTING, India.