Medtech Insight 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

Single-use device reprocessing FDA draft policy expected this summer.

This article was originally published in The Gray Sheet

Executive Summary

SINGLE-USE DEVICE REPROCESSING POLICY DEVELOPMENT BY FDA is being undertaken by a recently formed committee in the agency's Center for Devices and Radiological Health. Headed by Larry Spears, acting director in the Division of Enforcement III in CDRH's Office of Compliance, the committee expects to have a preliminary policy statement ready for presentation to the FDA commissioner's office by early summer.

Latest Headlines
See All
UsernamePublicRestriction

Register

MT005839

Ask The Analyst

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

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