FAQ
Most frequent questions and answers
Bravaura provides regulatory and product development support for food, dietary supplements, cosmetics, and medical devices. We help ensure your product is compliant and ready for market in the U.S., Canada, the EU, and Australia.
Yes! Whether you’re developing your very first product or expanding an existing product line into new markets, we offer tailored guidance—from product idea validation to labeling compliance and reformulation.
Absolutely. We specialize in multi-market compliance, including:
FDA (U.S.)
Health Canada (Canada)
EU regulations (EC/1223, EFSA, MDR)
TGA (Australia)
We’ll help ensure your labels, claims, and ingredients meet the specific requirements of each market.
Yes. We review or create your product label to ensure it meets all regulatory requirements (FDA, CFIA, EU, etc.) while maintaining strong branding. We also provide bilingual labeling for Canadian markets (English and French).
Yes, we can help you adapt formulations to comply with local regulations, especially when entering new markets like Canada (NHP/NPN) or the EU (Novel Food/Cosmetic Ingredient listings).
This online program includes step-by-step webinars, workbooks, and checklists covering product idea validation, branding, packaging, labeling, and compliance. It’s designed to help food founders and entrepreneurs launch with confidence.
Yes, expedited services are available upon request and subject to availability. Contact us to discuss your project timeline.
Of course. We respect your confidentiality and are happy to sign a Non-Disclosure Agreement before discussing proprietary or sensitive information.
Click “Book a Free Consultation” to schedule a discovery call. We’ll discuss your goals and recommend the best approach to move forward—whether it’s a one-time assessment or a full launch support package.
