I was referring to your opinion on here, none of us have the final say. If your opinion is important to the Company then good for you. If the FDA grants approval for these 15-second tests gearing up production and getting a sales force or distribution system in place will be a big undertaking given that the Company plans on selling 400 plus million units. Not only that, but the QC at the manufacturing level is also a major concern. I doubt many large pharmaceuticals could ramp up to hit those numbers. Is the FDA ISO contractor the Company has in Korea ready for this type of workflow?