The Cutting Edge of Medical Technology Content, Community & Collaboration
Time: March 15, 2019 from 10am to 11:30am
Street: 161 Mission Falls Lane, Suite 216,
Website or Map: https://www.compliance4all.co…
Phone: Event Manager
Event Type: webinar
Organized By: Adam Fleming
Latest Activity: Jan 25
This webinar will focus on the key areas that are most important for protecting the validity of data that is regulated by FDA, and is typically housed electronically in computer systems.
Why should you Attend:
This guidance was first issued in 1983, and the main points of focus remain consistent today, despite the number of years that have passed and the technology changes that have taken place.
Areas Covered in the Session:
FDA Regulatory Trends
FDA Response to Change
Recent FDA findings for companies in regulated industries
Recent trends in technology that need to be addressed in the CSV approach
Industry Best Practices
Who Will Benefit:
Clinical Data Scientists
Carolyn (McKillop) Troiano has more than 35 years of experience in the tobacco, pharmaceutical, medical device and other FDA-regulated industries. She has worked directly, or on a consulting basis, for many of the larger pharmaceutical and tobacco companies in the US and Europe, developing and executing compliance strategies and programs.
Event Fee: One Dial-in One Attendee Price: US$150.00
Compliance4All DBA NetZealous,