Biotech Consulting & Cross-Border Pharma Advisory.
Life science consulting for licensing, M&A, partnerships, and deal-making across global pharma and biotech.
The next decade of medicine will be written by partnerships that move across borders — not within them.
Strategic advisory across the full deal lifecycle.
Each engagement is led by senior advisors with first-hand operating experience across our three core regions. We work selectively, with a focused team, and stay involved from sourcing through close.
In-Licensing
Acquire rights to innovative therapeutics and technologies from global sources.
- Asset sourcing
- Scientific diligence
- Deal execution
Out-Licensing
Represent differentiated programs to qualified strategic buyers and partners.
- Buyer mapping
- Package preparation
- Terms negotiation
Strategic Partnerships
Build alliances for development, manufacturing, and commercialization.
- Co-development
- Cross-border manufacturing
- Joint commercialization
NewCo Formation
Spin assets into independent entities with global capital and dedicated focus.
- Carve-out structuring
- Capital syndication
- Governance design
Where our network runs deepest.
We advise across modalities and indications. These are the areas where our cross-border relationships, scientific depth, and recent deal flow are most concentrated.
Oncology
ADCs, bispecifics, targeted small molecules, and novel modalities.View →Immunology
Autoimmune, inflammation, and next-generation immunomodulators.View →Metabolic
GLP-1 combinations, NASH, and emerging cardiometabolic.View →Cell & Gene
CAR-T, allogeneic platforms, and gene therapy technologies.View →CNS
Neurodegeneration, psychiatry, and rare neurological indications.View →Rare Disease
Orphan therapeutics and ultra-rare development programs.View →Devices & Dx
Medical devices, diagnostics, and companion diagnostics.View →Digital Health
AI-led discovery, trial tech, and digital therapeutic platforms.View →A specialist advisor for life-science deal-making.
Decades of combined experience in pharma and biotech business development. Our specialized knowledge and tri-continental network make us the catalyst for life-changing collaborations.
Scope of engagement.
The mandates we run, the deal sizes we work, and the speed at which a partner-led team can move.
Selected thinking from the desk.
China clinical trials: cost, speed, and regulatory advantages
Run clinical trials in China and save 60% on costs with 2–5× faster enrollment. NMPA IND process, MRCT strategy for FDA acceptance, BIOSECURE Act clarification, and the China CRO landscape.
Continue reading →NMPA drug approval process: complete guide 2026
Dragon Pipeline / February - top deals from Asia this month
Capital access for biotech: routes to global syndicate
BioDeal Weekly / January wrap - out-licensing trends
Cross-border partnerships: the Asia to US corridor in 2026
Pharma deal intelligence, delivered.
The Asia → world deal feed.
Curated cross-border licensing, M&A, and partnership intelligence from Greater China, the corridor that's reshaping global pharma.
Every cross-border deal that mattered, in five minutes.
A Friday digest of the week's biggest licensing, M&A, and capital movements across pharma and biotech worldwide.