Zdrowie i gospodarka · 14/12/1998

FDA Announces Submission of Medical Device Information Collection for OMB Review

The Food and Drug Administration (FDA) has submitted a request for review of its proposed collection of information related to the Third-Party Review Program Under U.S./EC MRA, a medical device regulation, to the Office of Management and Budget (OMB) for compliance with the Paperwork Reduction Act of 1995.