Regulatory Support

NutriSciences have detailed knowledge of global legislation and regulations governing the food, beverage, supplement and 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 provide the most comprehensive and accurate information to our clients.

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

We achieve this 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 post-marketing changes, to complete regulatory dossiers for new active substances (i.e. Novel foods, Marketing Claims).
• 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 safety and/or efficacy database for regulatory submissions for new substances.

By using the expertise of NutriSciences 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 Labeling
• Health Claims

Click here for our "Regulatory Support" portfolio.