
Michael W. Porter
Founder & Executive ChairmanMore than twenty-five years building, acquiring and scaling regulated healthcare and specialty pharmaceutical platforms across the United States, Europe and international markets.
Headquartered in Zug, we operate the layer of this market that endures: controlled product identity, quality assurance, compliant sourcing, and physician and pharmacy access. Cannexa is our first therapeutic franchise. Our leadership team has built and scaled specialty pharmaceutical platforms across Europe and North America, and we apply that operating discipline here, deliberately, and by design.
Switzerland first, with selected European markets to follow as authorisations permit. Product development and availability are subject to applicable authorisation, prescription and pharmacy requirements.
An experienced board, named regulatory accountability and a quality system that reaches from source material to the pharmacy counter.
Altanova selectively licenses, partners and acquires around capabilities that strengthen regulated access, product differentiation and evidence. Every expansion is milestone-gated and must fit the quality system.

Michael W. Porter
Founder & Executive ChairmanMore than twenty-five years building, acquiring and scaling regulated healthcare and specialty pharmaceutical platforms across the United States, Europe and international markets.

Dr. Raghav Chari
Board Advisor, Product Development & Scientific StrategyThirty years in biopharmaceutical research, development and commercialisation across neurology, oncology, inflammation, metabolic disease and dermatology.

Ozgur Kilic
Board Advisor, Finance & Corporate OperationsMore than twenty years in finance, operations and strategy across global pharmaceutical companies and private equity-backed businesses in Europe and the United States.
Our operating model connects three areas: science and portfolio, quality, manufacturing, medical channel and patient access.
Standardised formulations and advanced delivery formats, supported by published evidence and real-world data, under specialty-pharma discipline.
PortfolioManufacturing and batch release are carried out by appropriately licensed partners in accordance with applicable Swiss regulatory requirements and EU GMP standards. Each batch is tested against the relevant product specifications using European Pharmacopoeia methods before release.
Quality & ComplianceCoordination with prescribing physicians, specialty licensed pharmacies and patient-support services creates a structured access model that supports patients throughout treatment, from the first prescription through ongoing care.
Patient AccessFor each therapeutic franchise, Altanova manages product strategy, quality, supply, medical affairs and patient access. Appropriately licensed partners carry out manufacturing, testing, logistics and dispensing, as well as cultivation where applicable.