Registered Biotechnology
Our biotech is certified by the FDA as a product that complies with the U.S. Food and Drug Administration’s Center for Devices and Radiological Health compliance policy entitled “General Wellness: Policy for Low Risk Devices ‘issued July 29, 2016” and has FDA Guidance 1300013 (UCM429674).
CE confirms Regulatory Compliance Assurance by confirming that our biotechnology is cleared under EC Directive 2014/30 / EU and RoHS Directive 2011/65. It confirms that our biotechnology complies with the general requirements: EN 61326-1:2006 EMC Requirements; EN 60950-1:2006+A12:2011; EN: 5502/55011/55024.
Intertek’s ETL certification program confirms that our biotechnology meets the necessary requirements: 1. Intertek Recognized ETL Component – 5000055; 2. UL std 60950-1; 3. Certified according to CSA std. c22.2.No.60950-1.
CCC confirms that our biotechnology meets the requirements of the Chinese Certificate of Conformity for electrical compliance.
The device used for our analysis is FCC certified, which confirms compliance with Part 15: Federal Communications Compliance for Electromagnetic Emissions.
The HS Code system confirmed that the necessary requirements are met and it was assigned a Harmonized Shipping Code – 903180 – Other Verification, Measuring Instruments, Apparatus and Machines.
Reliability and Accuracy
At ActiOnToday, we use the S-Drive device, which evaluates more than 96 epigenetic biomarkers to process and provide a complete and personalized epigenetic report based on the bioinformation found in the root of your hair.
The technology is ISO EN 13485: 2012 certified, with all the associated regulations, to provide the highest quality standard and guarantee the accuracy and reliability of the results.
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