Vatten Pharma

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Alfredo Bittar

Alfredo Bittar

Executive Director

Alfredo Bittar is a Executive Director at Vatten Pharma.

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Idea

Vatten Pharma is building a next-generation pharmaceutical platform focused on transforming cannabinoid and phytotherapeutic treatments through advanced nanotechnology. The company’s core idea is to overcome the absorption, safety, and cost barriers of existing CBD products by delivering pharmaceutical-grade, water-soluble formulations optimized for central nervous system (CNS) and chronic pain indications. By combining cutting-edge formulation science with a diversified product portfolio and a LATAM-focused expansion strategy, Vatten aims to redefine how cannabinoid-based therapies are prescribed, consumed, and scaled across regulated medical markets.


Challenge

Vatten Pharma is addressing the fundamental limitations of traditional oil-based CBD therapies, which suffer from low bioavailability, high patient burden, and poor treatment adherence. Conventional CBD oils achieve only 6–10% absorption due to first-pass liver metabolism, resulting in inconsistent dosing, delayed therapeutic onset, and significant waste of active ingredients. This inefficiency forces patients to consume higher doses, increasing monthly treatment costs and limiting long-term adherence. Additionally, oily taste, gastrointestinal discomfort, and imprecise dosing mechanisms create significant usability challenges, particularly for elderly patients and children.


Solution

Vatten Pharma is delivering a nano water-soluble CBD technology that bypasses first-pass metabolism and achieves near-complete absorption, making it up to 10x more potent than traditional oil-based products. Recognized by the body as water, the formulation enables rapid onset of action, consistent dosing, and significantly improved therapeutic efficacy at lower doses. The solution is tasteless, easy to administer by mixing with any liquid, and eliminates gastrointestinal discomfort, driving better patient adherence. Higher potency translates directly into lower cost per effective dose, improving affordability while meeting pharmaceutical-grade safety and quality standards required by physicians and regulators.



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