Zdrowie i gospodarka · 9.05.2016
Streamlining Regulations for Good Manufacturing Practices for Hearing Aids; Public Workshop; Extension of Comment Period
The Food and Drug Administration (FDA or we) is extending the comment period for the document entitled "Streamlining Regulations for Good Manufacturing Practices for Hearing Aids; Public Workshop" that appeared in the Federal Register of January 7, 2016. In the document, FDA requested comments on the appropriate level of good manufacturing practices (GMPs) regulation to ensure the safety and effectiveness of air-conduction hearing aid devices. The Agency is taking this action in response to requests for an extension to allow interested persons additional time to submit comments.