Pink Sheet 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

FDA updates on BPA activities

This article was originally published in The Tan Sheet

Executive Summary

Infant formula manufacturers are testing product samples on an ongoing basis to minimize bisphenol A in food contact applications and identify safe levels of the chemical. The Center for Food Safety and Applied Nutrition is analyzing several infant formula brands with an updated testing method, Mitchell Cheeseman, deputy director of the Office of Food Additive Safety, said at an FDA Science Board meeting Feb. 24 in Gaithersburg, Md. Recent testing of 57 samples found a range of 0.02 to 10.55 µg of BPA per kg of infant formula, which Cheeseman calls "comparable to the existing data" on formula products. He added that FDA encourages industry to follow a voluntary "code of practice" - essentially good manufacturing practices for producing and filling infant formula cans - "to minimize BPA migration from existing packaging materials into" the product. The presentation was part of an ongoing dialog about BPA's safety in food contact applications (1"The Tan Sheet" Feb. 16, 2009, In Brief)

You may also be interested in...



Science Board to convene in August

FDA's scientific advisory panel will meet Aug. 17 in Rockville, Md., to discuss plans for an "additional subcommittee for the review of research" at the Center for Food Safety and Applied Nutrition, as well as receive updates on the agency's assessment of bisphenol A (1"The Tan Sheet" March 2, 2009, In Brief)

FDA responds to Science Board’s BPA review

The agency is formulating a response to its Science Board's review of FDA's draft assessment of bisphenol A's safety in food contact applications. Associate Commissioner for Science Norris Alderson initially replied to the board in a December 2008 letter, agreeing that FDA should focus on BPA applications that might impact infants, including formula packaging (1"The Tan Sheet" Jan. 5, 2009, In Brief). According to a Feb. 9 release, FDA and Health Canada officials held a forum Jan. 30 with manufacturers from both countries to discuss ongoing BPA reduction efforts. FDA says an international regulatory consensus holds that BPA exposure through food packages does not pose a risk to the general population, but the agency continues to review research on the potential low-dose effects of BPA

Could Eledon’s Anti-CD40L Change Transplant Medicine?

Eledon Pharmaceuticals’ CD40 Ligand blocker has yielded impressive results for post-transplant immunosuppression and cutting-edge transplant doctors have also used it for pig-to-human kidney and heart transplants, opening up the field of xenotransplantation. 

Topics

Latest Headlines
See All
UsernamePublicRestriction

Register

PS102658

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