September 13, 2022

[Webinar]: What you need to know for compliance of your new ingredients in US, Canada, and EU / UK

Join experts from Nutrasource and RNI Consulting as they discuss: What You Need to Know For Compliance of Your New Ingredients.

Our speakers will discuss a variety of regulatory pathways including GRAS, NDIN, Novel Food and NHP Master File with regards to US, Canada, and EU / UK.


•Pathway identification and description
•Main Regulation(s)
•Competent Authority
•Categories of Product
•Registration Procedure
•Scientific and Analytical Data Required
•Exclusivity Following Approval
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Amy Mozingo, MS | VP, US Nutra Regulatory Sciences | Nutrasource

Ms. Mozingo is Vice President of US Nutra Regulatory Sciences. She has over 15 years of experience in industry and consulting, holds a certificate as a Preventive Control Qualified Individual (PCQI), and is trained and experienced in ingredient approvals (GRAS, NDIN, FAP, CAP), product labelling, formulation reviews, and current good manufacturing requirements for dietary supplements.

Tania John, M.Sc. | VP, NHP & Pharmaceutical Regulatory Sciences | Nutrasource

Ms. John brings 15 years of regulatory and quality experience in the Canadian Natural Health Product (NHP) space, including cross-functional support and project management. Tania, having worked with all categories, developed a niche for herself in the beauty from within and digestive care areas. As Vice President of NHP & Pharmaceutical Regulatory Sciences, Tania works closely with Nutrasource’s analytical, clinical, medical writing, business development, and marketing teams to ensure client objectives are exceeded through strong scientific substantiation and strategic partnership. She has a B.Sc. and M.Sc. from the University of Guelph, majoring in Nutrition & Nutraceutical Sciences and Food Safety & Quality Assurance, respectively. More recently, she became the Lead of the Global Prebiotic Association’s (GPA) Scientific & Technical Committee and is supporting several of its Working Groups, including Regulatory Affairs.

Keval Bhoola | UK Business Manager & Medical Affairs Consultant | RNI Consulting

Keval Bhoola is a Medical Affairs Consultant and the UK Business Lead based in RNI Consulting’s London office. He has experience working on the clinical assessment of health products with a strong focus on product strategy. Keval can assist with marketing authorisations of medical devices, novel foods, food supplements, herbal medicines and cosmetics, and is able to write a range of supporting clinical/scientific dossiers. Keval holds a Bachelor of Pharmacy (Hons) degree and a Postgraduate Diploma in Business in Health Management, both from the University of Auckland, New Zealand. Keval has extensive experience in the health industry, starting his career as a pharmacist before transitioning into medical devices and medical affairs.