The Changing Landscape Of Medtech Regulation

Posted by Britney Bartel, Marketing Manager on April 18, 2018

PLEASE JOIN US ON THURSDAY MAY 3RD FROM 3:00 PM TO 4:30 PM FOR “THE CHANGING LANDSCAPE OF MEDTECH REGULATION,”

UNIVERSITY ENTERPRISE LABORATORIES (UEL) WITH SPEAKER DR. VANESSA HAASE, ASSOCIATE DIRECTOR OF REGULATORY TOXICOLOGY FOR WUXI APPTEC INC., ST. PAUL, MN.

Where: UEL, 1000 Westgate Drive, St. Paul, MN 55114,

1st Floor Conference Room – South Entrance

Synopsis

From the FDA’s Guidance on ISO 10993 to the EU Medical Device Regulation, there have been significant changes lately that affect pre-clinical safety testing for combination products and medical devices. Staying up-to-date is crucial to the commercialization of your product.

If you're involved in R & D, Regulatory Affairs, Quality Control/Quality Assurance, or any part of product development - this seminar is for you!

Dr. Haause will speak about recent regulatory changes and resulting trends that are emerging.

There will be an open Q & A Session immediately following the presentation along with ample time for networking.

Register for the Event

Topics: Medical Device, Preclinical Safety, Biological Safety Testing, Regulatory