Pink Sheet is part 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

Nanomaterials public meeting

This article was originally published in The Tan Sheet

Executive Summary

FDA will conduct a public meeting Sept. 8 to discuss regulated products that may contain nanoscale materials and request public comment on how to implement the recommendations of the Nanotechnology Task Force Report, according to an Aug. 7 Federal Register notice. In the notice, the agency asks for comment on proper assessment tools to evaluate nanomaterials, manufacturing processes for products containing nanomaterials and for personal accounts of experiences with nanoscale materials. Comments are due Oct. 24. The Nanotechnology Task Force issued its recommendations to FDA in July 2007 (1"The Tan Sheet" July 30, 2007, p. 12)...

You may also be interested in...



FDA Nano Meeting Is Just The Beginning of Supplement, OTC Questions

Rather than draft a potentially "onerous rule" based on insufficient current information about the use of nanotechnology in dietary supplements, OTC drugs and other products, FDA needs additional safety data to determine if guidance is even necessary, a leading industry scientist says

Nanotech Report’s Recommendations Unsettling To Supplement Industry

Dietary supplement industry groups say an FDA panel's report citing the lack of information about working with nanotechnology should prompt the agency to be cautious about acting on the panel's recommendation to issue a guidance on using nano-materials in new dietary ingredients

QUOTED. 29 September 2020. Phil Brown.

ABHI’s Phil Brown believes the future of UK device regulation will be innovation-friendly and patient-responsive system – but doesn’t expect easy alignment with the EU. See what he had to say.

Topics

UsernamePublicRestriction

Register

MT142313

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