Date :
Place : United States, Los angeles
Contact Person:John Robinson
Description:
This workshop style training course is designed based on 30 year of regulatory affairs experience in preparing more than 150 successful U.S. FDA submissions for major medical device companies.Deadline for abstracts/proposals : 21st February 2017
Organized By :NetZealous DBA as GlobalCompliancePanel
Keynote Speakers : Subhash R Patel Regulatory Affairs & Quality Compliance Consultant, MD Reg Consulting, LLC Subhash Patel is an accomplished Regulatory Affairs Professional offering 30 plus year of experience in authoring, preparing and submitting more than 150 successful premarket submissions to U.S. FDA. He brings his expert knowledge and hands-on experience in developing a robust premarket submission that secures clearance or approval from U.S. FDA. He offers valuable tips and suggestions on �what w
Conference Highlights :Overview: This workshop style training course is designed based on 30 year of regulatory affairs experience in preparing more than 150 successful U.S. FDA submissions for major medical device companies. In these 2 days, the following essential elements of U.S FDA premarket submissions will be covered: 1. History and background of U.S FDA Laws and Regulations 2. Classify Your Device 3. Choose the Correct Premarket Submission for your device 4. Compile the Appropriate Information for your Pre
Venue :Four Points by Sheraton Los Angeles International Airport, Airport Boulevard, Los Angeles, CA, United States
Check the event website for more details.