Company

About Altanova

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.

Where we operate

Switzerland first, with selected European markets to follow as authorisations permit. Product development and availability are subject to applicable authorisation, prescription and pharmacy requirements.

How we are governed

An experienced board, named regulatory accountability and a quality system that reaches from source material to the pharmacy counter.

Corporate development

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.

Leadership

The experience behind the platform

Michael W. Porter, Founder & Executive Chairman, Altanova Pharma Group AG

Michael W. Porter

Founder & Executive Chairman

More than twenty-five years building, acquiring and scaling regulated healthcare and specialty pharmaceutical platforms across the United States, Europe and international markets.

Michael W. Porter

Founder & Executive Chairman

More than twenty-five years building, acquiring and scaling regulated healthcare and specialty pharmaceutical platforms across the United States, Europe and international markets. Michael W. Porter is Founder and Executive Chairman of Altanova Pharma Group AG in Zug, Switzerland, where he leads corporate strategy, governance, platform architecture and strategic partnerships. He co-founded Covis Pharma Group and served as its Chief Executive Officer, building the company into a top-ten global respiratory pharmaceutical platform with more than US$600 million in annual sales, more than 300 employees and commercial operations across more than 55 countries, while completing 23 M&A transactions. The Covis platform generated more than US$1.5 billion in distributed profit for its institutional sponsors across three monetization events. Across his career, he has led more than 25 life-sciences M&A and strategic transactions. Michael is Co-Founder and Managing Partner of PG Equity Group, the family office through which he and Liliana Gómez invest as operating partners in regulated healthcare, technology and critical-minerals businesses. He also serves as Independent Director and Audit Committee Chair of Freedom Metals Acquisition Corp., a Nasdaq-listed company, and as a director of restor3d, Pressio Spine and Huxley Medical, including Audit Committee Chair responsibilities at restor3d and Pressio Spine. He holds an MBA from Columbia Business School with a concentration in Finance and International Business.

Dr. Raghav Chari, Board Advisor, Product Development & Scientific Strategy, Altanova Pharma Group AG

Dr. Raghav Chari

Board Advisor, Product Development & Scientific Strategy

Thirty years in biopharmaceutical research, development and commercialisation across neurology, oncology, inflammation, metabolic disease and dermatology.

Dr. Raghav Chari

Board Advisor, Product Development & Scientific Strategy

Thirty years in biopharmaceutical research, development and commercialisation across neurology, oncology, inflammation, metabolic disease and dermatology. Dr. Raghav Chari advises Altanova on portfolio selection, formulation strategy and development planning. He currently serves as Chief Science Officer of Azurity Pharmaceuticals, where he is responsible for scientific strategy and development of the company's clinical pipeline. He previously served as Chief Innovation Officer of Covis Pharma, where he led research and development, and held senior leadership roles at Dr. Reddy's Laboratories and Promius Pharma. His expertise centres on 505(b)(2) and hybrid-medicine development, integrating formulation science, modelling, clinical pharmacology and late-stage development. Raghav began his career at McKinsey & Company, advising biopharmaceutical clients on strategy, licensing and M&A. He has contributed to more than 50 licensing, product-development and corporate transactions and has co-founded biotechnology companies working at the intersection of drug discovery and artificial intelligence. He holds a PhD in Physics from Princeton University and a BSc in Mathematics from the California Institute of Technology.

Nick Kelly, Board Advisor, Supply Chain & Technical Operations, Altanova Pharma Group AG

Nick Kelly

Board Advisor, Supply Chain & Technical Operations

More than twenty years in end-to-end global pharmaceutical supply-chain leadership across branded, generic and medical-device organisations, including as Chief Supply Chain Officer.

Nick Kelly

Board Advisor, Supply Chain & Technical Operations

More than twenty years in end-to-end global pharmaceutical supply-chain leadership across branded, generic and medical-device organisations, including as Chief Supply Chain Officer. Nick Kelly advises Altanova on supply-network design, supplier strategy, technical-operations readiness and operational resilience. He is Chief Supply Chain Officer of Adalvo, a global B2B pharmaceutical company supporting more than 170 partners across 140 markets. Nick previously served as Senior Vice President, Supply Chain at Covis Pharma, where he worked alongside Michael Porter for eight years and led end-to-end global supply-chain operations through M&A integrations, portfolio expansion and digital-transformation programmes. Earlier in his career, he held senior regional and global supply-chain roles at Cardinal Health, Teva Pharmaceuticals and Johnson & Johnson. His experience spans demand planning, procurement, logistics and customer service, with particular depth in supplier relationships, contract negotiation, sustainable sourcing and supply-chain risk management.

How we operate

Our operating model connects three areas: science and portfolio, quality, manufacturing, medical channel and patient access.

01 · Science & Portfolio

Standardised formulations and advanced delivery formats, supported by published evidence and real-world data, under specialty-pharma discipline.

Portfolio
02 · Quality & Supply

Manufacturing 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 & Compliance
03 · Medical Channel & Patient Access

Coordination 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 Access

For 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.