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Resources

Quality

FDA Registration

Aquila Bioscience have been successfully registered as a foreign manufacturing facility with FDA under Owner/ Operator Number 10074735

The ABD Wipe product is registered with FDA under device listing D405606.

Aquila Bioscience are now permitted to market and sell the ABD Device in the US market.

CE Mark

Path to CE mark is underway and is expect to be completed in 2020

Media

Interview with Lokesh Joshi, Founder of Aquila Bioscience

How ABD Technology Works