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NNHPD Regulatory Updates: Name Change, Three Class System Finalized and Pilot Program for Monograph Attestation for OTC
September 8, 2014 By
NNHPD released many updates recently including: changing the name of the Directorate, finalizing the 3 Class review system for NHPs, announcing a 6 month pilot program for NHPs that fall […] Read More >>
NHPD Releases Quarterly Snapshot for Q 4, FY 2013-2014 and Advises of New Monographs to be Posted
June 9, 2014 By
On May 21st,  the NHPD released the Quarterly snapshot for Q4 indicating more streamlined review, aided by the release of new monographs. Readers of dicentra’s Regulatory Updates will know that […] Read More >>
SPECIAL ALERT: NHP Compliance and Enforcement Transition: Phase I ending December 1, 2013
November 8, 2013 By
November 8, 2013 Phase I of the NHP Compliance and Enforcement transition period is ending December 1, 2013. Companies have been advised to ensure that they are familiar with and […] Read More >>
dicentra’s Regulatory Webinar – Q1: March 26, 2013
March 26, 2013 By
March 26, 2013: dicentra conducted its first webinar of 2013. Critical American and Canadian updates including FDA’s proposed rules to amend cGMPs for food facilities under FSMA, the FDA’s Draft […] Read More >>
Update: Oil of Oregano and Carvacrol
March 4, 2013 By
NHPD revises maximum daily limit of carvacrol for natural health products containing Oil of Oregano as a medicinal ingredient. Oil of oregano, derived from the species of Origanum spp., is […] Read More >>
dicentra’s NHP Regulatory Update 2012 – Q3
September 18, 2012 By
Topics covered: Canada: Consultations & Regulatory Initiatives Food Safety & Initiatives United States: Proposition 37 – Genetically Engineered Foods, Labeling, Initiative Statute Energy Drink Controversey Status of Draft NDI Guidance [&helli Read More >>
dicentra is now a Proud Sponsor to Europe NOW
June 30, 2012 By
Contact us to book a meeting or drop by our booth to discuss how dicentra can help you with your regulatory and scientific affairs concerns. dicentra provides regulatory and scientific […] Read More >>
The Dietary Supplement Industry Can Breathe a Sigh of Relief, For Now
June 25, 2012 By
By Heather VanBlarcom General Counsel & Senior Regulatory Specialist for Dietary Supplements We can breathe a sigh of relief thanks to Senate supplement-industry champions Tom Harkin (D-IA) and Orrin Hatch […] Read More >>
If You Think the FDA’s cGMPs Don’t Apply to You, Think Again!
April 30, 2012 By
By Heather Van Blarcom General Counsel & Senior Regulatory Specialist – USA If your name is on the label of a dietary supplement product that you market and distribute, you […] Read More >>

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