- This event has passed.
Consulting 301 – FDA Medical Device Regulatory Process – How a consultant helps your company manage and adhere to FDA guidance
Topic: Consultants Series Part 3
Consulting 301 – FDA Medical Device Regulatory Process – How a consultant helps your company manage and adhere to FDA guidance
Consultant: David Connor
Meeting starts at 7:00 PM.
Open to the public: Networking from 6:30PM – 7 PM.
Event Description:
The FDA medical device regulatory process will be discussed. You do not have to be familiar with the FDA regulatory process to get benefit from this meeting. This is an overview of the regulatory process and how a consultant will add value, whether you need to implement a regulatory process or have an existing process. Come find out more about the process and where consultants have helped identify mistakes that often occur in this complicated process.
No Prior Knowledge Needed – You do not need to know anything about the regulatory process in order to understand this talk. You do not need to be a consultant. Anyone that wants to gain knowledge about this process should come.
Day/Time: Dec 3, 6:30 – 8:15pm (EST)
Location: Zoom