Online Training 2015 - Registration & Listing, FDA Inspection Strategies and Compliance Initiatives ? Medical Device. - By Compliance Global Inc

Overview:
Have you ever wondered about the FDA strategies for scheduling inspections and pursuing compliance plans? This seminar will provide clarity around those issues from a compliance expert with over 30 years’ experience in inspection and compliance management.
Why Should You Attend:
Many companies do not know what they don’t know when it comes to dealing with the FDA. By not understanding how FDA uses registration and listing data, these companies sometimes fail to address key issues in response to fda 483s and Warning Letters and fail to manage inspections to reduce their overall risk. Here is your chance to better understand how FDA thinks and operates and what their key areas of focus and priority are from a former Compliance insider.
Areas Covered in the Session:
Registration and Listing regulatory requirements, process, and how FDA uses this data will be discussed. FDA strategic direction and how they reach decisions in developing inspection and compliance plans will be discussed.
Learning Objectives:
? Registration and Listing process and requirements.
? FDA inspection planning activities
? Compliance strategies
Who Will Benefit:
? VP’s and Directors in Regulatory Affairs
? VP’s and Directors in Quality Assurance
? Regulatory Affairs Managers and Professionals
? Quality Managers and Professionals
? Small Business Owners
Level:
Beginner
For more detail please click on this below link:
https://www.complianceglobal.us/product/700084
Email: referrals-AT-complianceglobal.us
Toll Free: +1-844-746-4244
Tel: +1-516-900-5515