Cantox Food & Nutrition Group professionals have detailed knowledge of global legislation and regulations governing food, supplement, and other food-related products. We conduct on-going surveillance of regulatory policies and practices as they change or develop, which allows us to achieve an unparalleled understanding of the intricacies and processes of regulatory agencies and requirements and provide appropriate information to our clients.

Whether you plan to market your product in the North America, Europe, Asia, or other jurisdictions worldwide, our team develops superior regulatory strategies to suit your needs based on the product type, submission requirements, and jurisdiction, thus ensuring success in a timely fashion. We can assist by:

• Drawing on, and integrating, comprehensive regulatory and scientific experience into the design of regulatory strategies to meet international regulatory requirements and pre-empt regulatory concerns and questions
• Preparing submissions, from pre-meeting packages and postmarketing changes, to complete dossiers for new active substances for regulatory agencies worldwide.
• Liaising with regulatory agencies, including facilitating meetings, and providing independent, third-party critical advice on and responses to regulatory issues;
• Developing global monitoring programs to ensure that products remain compliant in changing regulatory climates
• Advising, planning, and assisting in preclinical and clinical study design and monitoring work with contract research organizations (CROs) to ensure completeness of the safety and/or efficacy database for regulatory submissions for new substances

By using the expertise of our team at CANTOX your timelines and budget can be met.

Product-specific submission support is provided for:

• Food additives & ingredients, including Generally Recognized As Safe (GRAS) substances and Novel foods
• Supplements and Natural Health Products
• Packaging and Labelling
• Products for Animals
• Health Claims