Biotech & Pharma Business Development

We work across the full BD lifecycle — asset scouting and in-licensing, technical and commercial due diligence, valuations, out-licensing and partnering, deal negotiation support, and academic commercialization — for pharma and biotech companies at every stage, life science investors, and research institutions.

Many of our clients are early-stage or virtual biotechs where leaders are wearing multiple hats - a CMC specialist now responsible for partnering, a clinical development lead navigating their first fundraise - and need experienced BD support without building a full internal team. And many engagements combine multiple disciplines: a scouting engagement leads to DD on a shortlisted target, which leads to a valuation to support negotiations. Having one firm with depth across all of these reduces handoff risk and accelerates decision-making.

Why the right BD partner matters

Buy-side — ensuring risk is accurately assessed across every dimension so you have a clear basis for a go/no-go decision and confidence that the deal is priced appropriately

Sell-side — positioning your asset to achieve the highest value with the right partner, and ensuring there are no surprises when their DD team arrives

Investor — investing in a program with a clear understanding of its true risk profile, without hidden challenges that surface after you've committed capital

We work across the full BD lifecycle — asset scouting and in-licensing, technical and commercial due diligence, valuations, out-licensing and partnering, deal negotiation support, and academic commercialization — for pharma and biotech companies at every stage, life science investors, and research institutions. Many of our clients are early-stage or virtual biotechs where leaders are wearing multiple hats — a CMC specialist now responsible for partnering, a clinical development lead navigating their first fundraise — and need experienced BD support without building a full internal team. And many engagements combine multiple disciplines: a scouting engagement leads to DD on a shortlisted target, which leads to a valuation to support negotiations. Having one firm with depth across all of these reduces handoff risk and accelerates decision-making.


Our Business Development Services

Five interconnected service lines spanning the full BD lifecycle.

1

In-Licensing & Asset Scouting

Systematic identification of licensing and acquisition targets that match your strategic criteria. We work alongside your internal BD team — or operate as an extension of it — to surface opportunities not yet visible in pipeline databases. Engagements range from targeted therapeutic area searches to multi-year retained partnerships.

Literature, patent, and clinical trial registry screening Direct outreach to early-stage biotechs and academic groups TTO and licensing professional networks Conference attendance and partnering meetings Cross-border scouting (US, Europe, Asia) Distressed asset and discontinued program screening

Engaged by pharma companies supplementing internal scouting capacity, biotechs seeking complementary pipeline assets to strengthen a fundraising story, and investors surveying a therapeutic landscape before committing to a thesis. We scout across geographies, with particular strength in US-Europe cross-border work.

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2

Due Diligence

Comprehensive technical and commercial assessments that give you the full picture before making a transaction decision. Our DD teams are assembled for precise relevance — an oncology gene therapy gets evaluated by oncology and gene therapy development experts, not generalists. We can mobilize quickly for competitive situations and deliver expedited assessments when deal timelines require it.

Clinical data and scientific assessment Regulatory strategy and agency correspondence CMC readiness and manufacturing risk IP position and freedom-to-operate Commercial viability and competitive positioning DD readiness for incoming diligence

Clients range from large pharma evaluating in-licensing candidates to VCs conducting early-stage investment DD to PE firms assessing later-stage acquisitions.

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3

Pharma & Biotech Valuations

Independent, model-driven valuations grounded in development reality. We build valuations that reflect actual development costs, timelines, and probabilities of success — informed by our consultants' firsthand experience running clinical programs and managing regulatory submissions.

Risk-adjusted NPV models (single-asset and pipeline) Revenue forecasts and scenario analyses Royalty stream and monetization analyses Deal benchmarking and term sheet appraisals Monte Carlo simulations for high-uncertainty programs Independent valuation critiques and second opinions

Used by pharma BD teams setting deal terms, biotechs establishing negotiating positions, investors sizing portfolio opportunities, and boards requiring independent valuation opinions.

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4

Out-Licensing, Partnering & Deal-Making

End-to-end support for companies seeking licensing partners, preparing for transactions, or navigating deal negotiations. This is a core area of our practice, particularly for early-stage and growth-stage biotechs. On the sell side, we handle the full out-licensing process from preparation through close. On the buy side, we help pharma and biotech companies structure deals, assess term sheets, and evaluate competitive bids. Our consultants understand what both sides of a transaction look for — many have led BD functions or negotiated licensing deals themselves.

Data room build and partnerability assessments Mock DD to identify vulnerabilities pre-negotiation Pitch deck and licensing package preparation Partner identification, prioritisation, and outreach Valuation, deal comps, and term sheet support Buy-side deal structuring and bid evaluation

Engaged by biotechs preparing their first licensing deal, companies managing multi-party competitive processes, pharma teams structuring in-licensing terms, and investors supporting portfolio companies through partnering.

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5

Academic Commercialization

Turning academic research programs into investable opportunities. Having worked with 40+ universities globally — and simultaneously serving pharma, biotech, and investor clients — we bring real-time insight into what licensees and VCs are actually looking for and what will survive their scrutiny.

Invention disclosure triage and prioritisation Commercial potential and market assessments Development plans bridging academic to industry standards Partnerability assessments and mock DD Licensing, spin-out, and partnership support Patent strategy and go/no-go decisions

Engaged by technology transfer offices managing large disclosure portfolios, research groups preparing specific programs for industry engagement, and university leadership evaluating commercialization strategy across departments.

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BD Powered by Development Experience

Most BD advisory firms staff transactions with analysts and strategists. Alacrita staffs them with people who have actually developed products — former CMOs who know what clinical data should look like, regulatory leaders who've been through agency meetings, CMC heads who understand manufacturing risk, and commercial executives who've launched drugs. Every dimension of a transaction — scientific, clinical, regulatory, commercial, financial — is assessed by someone who's done that work firsthand.

Many of our BD engagements naturally span multiple services. A scouting engagement surfaces a promising target; we conduct DD on the shortlist; the DD feeds directly into a valuation model; the valuation informs term sheet negotiations. On the sell side, we prepare a biotech for partnering by running mock DD, building the data room, valuing the asset, and then supporting outreach and negotiation. Having one firm with continuity across these stages — and the technical depth to execute each — means less rework, fewer handoffs, and faster decisions. It also means we can help with what comes after the deal: our product development, clinical, regulatory, and CMC teams can pick up where the BD engagement leaves off.


Who Engages Us

Early-Stage & Virtual Biotechs

A core client segment. Many of our biotech clients are lean teams where leaders have deep technical expertise but are taking on BD responsibilities for the first time — a CMC specialist now responsible for finding a manufacturing partner, a clinical lead navigating their first licensing discussion. We provide the BD experience and process so they can focus on the science. From data room preparation and mock DD through partner identification, valuation, and deal close.

Pharma BD Teams

Supplementing internal BD capacity with targeted scouting, DD, and valuation support. Many pharma clients engage us on a retained basis across multiple engagements per year, or maintain an ongoing scouting function across specific therapeutic areas and geographies.

Life Science Investors

Technical due diligence and independent valuations for VCs, PE firms, family offices, pension funds, and accelerators. We calibrate depth and language to the audience: scientific thesis validation for early-stage VCs, commercial viability assessments for later-stage PE, and investment committee-ready reports for institutional investors.

Universities & TTOs

Commercialization strategy, technology evaluation, development planning, and licensing support for research programs. We've worked with 40+ universities globally, bringing real-time insight into what industry licensees and investors are looking for. Engagements range from single-disclosure evaluations to ongoing portfolio prioritisation.


Business Development Case Studies


Our Thinking on Business Development

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Common Questions

How is Alacrita's BD consulting different from a boutique advisory or investment bank?

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We're not a financial advisor — we're a technical and scientific consulting firm with deep BD expertise. Our assessments are powered by the same 350+ specialist network that supports our drug development work. Due diligence is conducted by consultants who have developed products in the relevant therapeutic area and modality, not generalist analysts. Valuations are built on development assumptions from people who have run clinical programs and managed regulatory submissions.

Can Alacrita support long-term scouting engagements, or only project-based work?

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Both. Many of our scouting clients engage us on retained, multi-year partnerships where we function as an extension of their internal BD team. We also take on targeted, time-limited searches for specific opportunities. Engagements have ranged from focused 3-month searches to retained relationships lasting 8+ years.

What therapeutic areas and modalities do your BD consultants cover?

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Our network spans 22 disease areas and 18 product modalities. We have particular depth in oncology (209 specialists), immunology, CNS, rare diseases, cell and gene therapy, small molecules, and antibodies/ADCs. For any given transaction, we match consultants with direct experience in the relevant science.

How does Alacrita handle confidentiality across BD engagements?

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Every engagement operates under its own confidentiality agreement. Consultant teams are siloed — a consultant working on DD for one client has no visibility into other engagements. Our core team screens for conflicts before accepting any new assignment. If a potential conflict arises — for example, a DD target that is also an existing Alacrita client — we disclose the situation to both parties and either decline the engagement or, if both parties agree to proceed, assign entirely separate teams with no overlapping personnel. We do not accept engagements where we cannot maintain clear separation.

Can Alacrita provide valuations that can be used in board or investor presentations?

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Yes. Our valuation models are built to withstand scrutiny from boards, investment committees, and transaction counterparties. We use risk-adjusted NPV approaches with transparent assumptions, sensitivity analyses, and scenario modeling.

Can Alacrita support both sides of a transaction?

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Not simultaneously. We work for one party per transaction. However, our experience on both buy-side and sell-side engagements means we understand what both parties look for, which strengthens our work regardless of which side we're advising.

Is Alacrita a staffing agency or expert network?

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No. Alacrita is an integrated consulting firm with a permanent core team of senior industry operators who lead engagements and maintain client relationships. That core team draws on a network of 350+ specialist consultants who work for Alacrita — not as independent contractors placed into your organisation. Clients contract with Alacrita. We assemble teams, manage engagements, review deliverables, and maintain accountability throughout.

Does Alacrita work with early-stage biotechs and virtual companies?

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Yes — early-stage and virtual biotechs are a core client segment. Many of our BD clients are lean teams where leaders have deep technical expertise but are taking on BD responsibilities for the first time. We provide experienced BD support across the full process — from data room preparation and mock DD through partner identification, valuation, and deal close — without requiring you to build a full internal BD team.


Tell Us About Your Opportunity

Whether you have a specific transaction in mind or you're exploring options and aren't sure where to start, we're happy to talk. Tell us about your asset, your timeline, and what you're trying to achieve — we'll help scope the right approach.