Scrip is part of Pharma Intelligence UK Limited

This site is operated by Pharma Intelligence UK Limited, a company registered in England and Wales with company number 13787459 whose registered office is 5 Howick Place, London SW1P 1WG. The Pharma Intelligence group is owned by Caerus Topco S.à r.l. and all copyright resides with the group.

This copy is for your personal, non-commercial use. For high-quality copies or electronic reprints for distribution to colleagues or customers, please call +44 (0) 20 3377 3183

Printed By

UsernamePublicRestriction

Medical device reporting final reg

This article was originally published in The Gray Sheet

Executive Summary

Is at the office of general council, according to Chester Reynolds, director of the post market management staff at the Center for Devices and Radiological Health's office of compliance and surveillance. Speaking at the BioEast Conference in Washington, D.C. on Jan. 26, Reynolds said: "If we avoid problems, [the regulation] should be final sometime in...May or June." A tentative final MDR regulation was published in the Nov. 27, 1991 Federal Register ("The Gray Sheet" Nov. 25, 1991, p. 1)....

Latest Headlines
See All
UsernamePublicRestriction

Register

MT000146

Ask The Analyst

Ask the Analyst is free for subscribers.  Submit your question and one of our analysts will be in touch.

Thank you for submitting your question. We will respond to you within 2 business days. my@email.address.

All fields are required.

Please make sure all fields are completed.

Please make sure you have filled out all fields

Please make sure you have filled out all fields

Please enter a valid e-mail address

Please enter a valid Phone Number

Ask your question to our analysts

Cancel