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CHPA appreciates the opportunity to provide information relevant to the assessment of the evidence of the potential developmental neurotoxicity of fluoride.

Nov 24, 2015

These comments supplement oral remarks made at the April 20, 2015 hearing regarding the regulatory framework for homeopathic drug products.

Oct 9, 2015

CHPA is generally supportive of the revision proposal to update and clarify the Chapter. We would however request that the implementation be delayed for 24 months.

Jul 30, 2015

CHPA appreciates the opportunity to provide comments on the FDA’s draft guidance for industry entitled “Formal Meetings Between the Food and Drug Administration and Sponsors or Applicants of Prescription Drug User Fee Act Products”.

Jun 3, 2015

FDA intends to expand the scope of Redbook to include chemical safety assessments for all products over which FDA's Center for Food Safety and Applied Nutrition has statutory authority. We urge FDA to provide clear and specific guidance for applying these principles within each particular context.

May 8, 2015

Please accept this letter as an official request from the CHPA to participate in the selection process for nonvoting industry representatives for several public advisory committees for the Center for Drug Research & Evaluation.

Apr 15, 2015

Letter to Principal Scientific Liaison, U.S. Pharmacopeia, regarding Proposals for Developing Compendial Quality Standards for OTC Drugs.

Apr 3, 2015

These comments touch on several of the goals identified by ODS in the Progress Report.

Mar 6, 2015

CHPA appreciates the opportunity to provide the Office of Dietary Supplements (ODS) with comments on their Strategic Plan 2010-2014 Progress Report.

Mar 6, 2015

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