When I first started out, this was giving me sleepless nights. I didn’t have anyone to turn to, and there was almost no information available on the internet, and no real experts to hire. This is the reason I started this company.
A food supplement/dietary supplement has to be notified at the regulatory authorities. Which is the exact reason why the labeling and the branding comes at this point in the “building a food supplement brand” sequence.
If the regulatory authorities refuse your food supplement, this means that you can not enter this market. If you try to enter with a completely finished product, it costs a lot of money to pivot to another market, or pivot the label and the branding and the formula to said countries needs.
So we notify the regulatory authorities first, and then build out the complete product. If you know the constraints you have to work with regarding health claims and marketing messaging, you can actually build a products that sells.
A typical list of what the regulatory authorities want to see when you send them your notification dossier:
- A COA of raw ingredients and a COA of the end product
- Instructions of use
- The source of the instructions of use
- Any other notification grant(s) from other countries
- Your packaging
- Health claims that you are planning to use
- Disclaimers
- GMP/FSC22000/HACCP certificates of the manufacturer partner