Navigating through Maze of In-vitro Diagnostics (IVD) Regulations: A systematic approach from Regulatory Strategy to Regulatory Approvals in U.S./Europe/Canada

Meeting has expired

Organizer: 
Meeting Description: 

In-vitro Diagnostics (IVD) products provide critical information on patient’s health condition, based on which the healthcare provider develops and administers treatment plan. Although IVDs are medical devices, they are regulated under a separate set of regulations in U.S., Europe, and Canada.

This 2 day interactive course on in-vitro diagnostics is structured to understand the different set of IVD regulations, how to navigate through this maze of IVD regulations, and to win regulatory approvals. This In-vitro Diagnostics (IVD ) course will make the attendees understand the IVD regulations and develop regulatory strategies that secure regulatory approvals.

Specialty: 
Radiology - Diagnostic
Country: 
United States
Map: 
United States (Show on map)
Start Date: 
09/16/2021
Time:
11:00 AM
Finish Date: 
09/17/2021
Time:
6:00 PM
Forgot/reset password
Sign in
Candidate registration
text.employer_info
Sign in
Advertiser registration
Login
Candidate registration
Advertiser registration
Login
Candidate registration