Ann: Firebrick Phase 3 Trial Closes with 500 Subjects, page-10

Thank you, Earth Angel.
I agree with everything you said, including the potential BOOM! However, please note that registration in Europe will take considerably longer than 3 months. Unlike medical devices, which can benefit from rapid approval in Europe, Nasodine is a medicine and will be evaluated much more thoroughly for quality, safety and efficacy. Realistically, we should expect the process to take at least 12 months. For your reference, here's a link to the timetable for EMA review:
https://www.ema.europa.eu/en/human-regulatory/marketing-authorisation/evaluation-medicines-step-step#:~:text=The%20assessment%20of%20a%20marketing,of%20a%20marketing%20authorisation%20application.