Retailers, Brands, and Distributors who have heard my sales pitch know I use "Red Dye # 3" as an example of regulatory challenges that demand more helpful and intelligent product data tools.
Today the FDA officially is repealing the color additive regulations that permit the use of FD&C Red No. 3 in foods (including dietary supplements) and ingested drugs.
I cite Red Dye # 3 as a product data challenge because for more than 30 years the reporting rules on this single food and drug additive have constantly changed.
Driven by consumer concern, the regulatory and reporting rules on Red Dye # 3 vary by country, state, retailer, and distributor.
From a supply chain perspective, managing these changes - for a single, well-known product attribute - is a costly challenge. Imagine the job of correctly addressing reporting and regulatory changes across hundreds of products moving to dozens of countries, all 50 states, and hundreds or thousands of retailers.
That job is not just hard, it's impossible (for humans).
Oh, and today's FDA rule change (Docket No. FDA-2023-N-0437) is 21 pages long.
Most Retailers, Brands, and Distributors will hope their existing reporting and data management tools are sufficient to satisfy today's FDA rule change.
Maybe.
Some Retailers, Brands, and Distributors will add additional consulting or full-time resource to understand and manage the implications of the rule change.
Some will simply ignore the rule change and absorb fines and customer churn.
But, some Retailers, Brands, and Distributors will simply add a new FDA validation to their nutrād Smart Pipes or Smart Portal instance and be instantly compliant with the FDA rule change.
Curious to know what group you want to be in.