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

Date : 11th March 2021 to 12th March 2021

Place : United States, San Jose

Website :https://www.complianceonline.com/in-vitro-diagnostics-ivd-regulatory-approvals-in-us-europe-canada-seminar-training-80148SEM-prdsm?channel=allconferencealerts

Contact Person:Ashutos Swain

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.

Navigating through Maze of In-vitro Diagnostics (IVD) Regulations: A systematic approach from Regulatory Strategy to Regulatory Approvals in U.S./Europe/Canada will be held in San Jose,United States on date 2021-03-12

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Deadline for abstracts/proposals : 1st March 2021

Keynote Speakers :

Check the event website for more details.