Medtech Insight is part of the Business Intelligence Division of Informa PLC

This site is operated by a business or businesses owned by Informa PLC and all copyright resides with them. Informa PLC’s registered office is 5 Howick Place, London SW1P 1WG. Registered in England and Wales. Number 8860726.

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
UsernamePublicRestriction

REMOVAL AND CORRECTION REPORTING BY DISTRIBUTORS IS "NOT NECESSARY,"

This article was originally published in The Gray Sheet

Executive Summary

REMOVAL AND CORRECTION REPORTING BY DISTRIBUTORS IS "NOT NECESSARY," the Health Industry Distributors Association argues in recent comments on FDA's proposed rule governing reports of removals and corrections by manufacturers, distributors and importers. The organization "questions whether the proposed regulation is really necessary or whether it is simply duplicating what is already being achieved by [other] reporting requirements of the Safe Medical Devices Act of 1990."
Advertisement
Advertisement
UsernamePublicRestriction

Register

MT002563

Ask The Analyst

Please Note: You can also Click below Link for Ask the Analyst
Ask The Analyst

Your question has been successfully sent to the email address below and we will get back as soon as possible. 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