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Service · Out-Licensing

Bring your asset to market with focus and full control.

PharmaSync helps asset owners position differentiated science, qualify the right strategic buyers, run confidential outreach, and negotiate structures that protect long-term value across the corridor.

PharmaSync cross-border out-licensing advisory
ModelSell-side

Positioning, buyer mapping, outreach, and term support.

ProcessSelective

Qualified counterparties, never broad-blast outreach.

MaterialsData-led

Non-confidential teaser, deck, data-room logic, and Q&A file.

DisclosureNDA-first

Staged gates protect identity, science, and intent.

What we deliver

A credible story for the buyers who should already care.

Asset positioning

We build the strategic narrative around differentiation, evidence, residual risk, and exactly where the asset fits a buyer’s portfolio.

Buyer mapping

We identify strategic and financial counterparties with the mandate, capability, and timing to engage seriously rather than browse.

Process management

We coordinate teasers, NDAs, data-room access, management calls, Q&A, and structured feedback loops end to end.

Term negotiation

We shape structure, economics, retained rights, diligence obligations, governance, and a clear path to signature.

Why PharmaSync

We make the asset easy to understand without flattening the science.

01

Scientific translation

Dense data becomes buyer-relevant proof points and honest risk disclosures.

02

Buyer discipline

Outreach is limited to counterparties with a real strategic reason to act.

03

Process control

Confidentiality, materials, and Q&A cadence are managed deliberately, not reactively.

04

Term focus

We protect value in the clauses that still matter long after the press release.

Process
01

Prepare

Validate the data package, sharpen positioning, and set the rules of the process.

02

Qualify

Map buyers and rank them on fit, capability, timing, and decision authority.

03

Engage

Run teasers, NDAs, data-room access, Q&A, and structured buyer meetings.

04

Close

Compare offers, negotiate terms, and drive signature readiness.

Diligence framework
01

Evidence hierarchy

Separate decisive data from supportive but non-critical evidence before buyers see it.

02

Differentiation

Clarify where the asset wins and where buyers will push back hardest.

03

Regulatory story

Make agency path, precedent, and open questions explicit and defensible.

04

CMC story

Frame manufacturing readiness and transfer risk before they become objections.

05

Market logic

Connect target population, standard of care, and strategic portfolio fit.

06

Terms range

Set realistic economics and rights packages well before the first offer lands.

Geography desks

China & Asia buyers

Strategic pharma, regional specialty players, and platform companies seeking differentiated rights.

Europe & Gulf capital

Companies and investors able to fund development, manufacturing, and regional launch paths.

US strategic buyers

Portfolio-driven pharma and biotech teams operating against defined therapeutic mandates.

Deal structures
StructureWhen it fitsPressure points
Regional licenseOwner wants to retain core geography while extending reach.Territory, field, diligence, supply, and data-sharing rights.
Global licenseBuyer is best placed to own full development and market path.Economics, transition, retained rights, and governance.
Co-developmentBoth parties contribute resources or know-how.Cost share, control, escalation, and future opt-in rights.
Option dealFurther evidence is needed before full commitment.Trigger data, exclusivity, option fee, and exercise mechanics.
Therapeutic coverage
01

Oncology

Targeted assets and novel modalities.

02

Immunology

Inflammation and autoimmune programs.

03

Metabolic

Cardiometabolic and NASH assets.

04

Cell & Gene

Cell therapy, gene therapy, and enabling platforms.

05

CNS

Neurodegeneration and psychiatric disorders.

06

Rare Disease

Orphan and ultra-rare indications.

07

Devices & Dx

Companion diagnostics and device-led assets.

08

Digital Health

Trial tech, DTx, and AI-enabled platforms.

Case studies
Cell therapy

Buyer map for platform rights

Segmented strategic buyers by manufacturing capability, clinical appetite, and territory value.

Oncology

Data-room rebuild

Reorganized a fragmented package into a buyer-ready structure before any outreach.

Diagnostics

Partner process reset

Shifted an unfocused process toward buyers with companion diagnostic infrastructure.

FAQ
How many buyers do you contact?
Only the number justified by the asset and the strategy. A narrow, qualified process almost always protects value better than broad outreach.
Do you prepare the non-confidential package?
Yes. We build or refine the teaser, management deck, data-room logic, and Q&A materials.
Can you help us compare competing offers?
Yes. We compare headline economics, risk transfer, retained rights, obligations, governance, and certainty of close.
Engagement

Take the asset to the buyers who can actually move.

Contact us ->NDA-first · Response within 24 hours