Our Services
Product Development

Planning and executing development programs across therapeutic areas and modalities, with a specialist, fractional CXO leadership, or a full virtual team.

Opportunity Mapping

Preclinical Strategy & Execution

Clinical Development

Clinical Operations & Trial Management

Regulatory Affairs

CMC Consulting

CDMO & CRO Selection & Management
Enterprise Development

The strategic and operational foundations to advance and fund your programs, from interim C-suite leadership to business planning and platform strategy.

Business Plans & Fundraising Support

Interim Chief Medical Officer

Virtual Biotech Support

Technology Platform Strategy

Launch Planning
Business Development

Buy-side and sell-side support for pharma, biotech, and investors, from asset scouting and due diligence through valuations, partnering, and deal close.

Due Diligence

Due Diligence Training

Valuations

In-Licensing & Asset Scouting

Out-Licensing, Partnering & Deal-making

Academic Commercialization
Investors and Law Firms

Scientific, strategic, and operational support across the investment lifecycle, and expert witnesses with the technical or commercial depth a case requires.

Investor Services

Expert Witness Services
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Who We Serve
Organizations we work with
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Disease Area

CNS

Digestive & GI

Endocrine & Metabolic

Fibrosis

Hematology

Immunology

Oncology

Respiratory

Other Disease Areas
Product Modality

Antibodies, ADCs

Cell Therapies

Drug Discovery Platforms

Gene Therapies

Microbiome Drugs

Peptides & Proteins

Radiopharmaceuticals

Small Molecules

Other Product Modalities
Our Company
Since 2009, Alacrita’s core team and associate consultants have supported biotechs, pharma companies, investors, and universities on development programs, deals, and company building, from Cambridge, MA and London.
More about Alacrita
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Latest

Whitepaper Deterministic Intelligence in a Probabilistic World The clinical record behind AI-derived drugs is smaller and more divided than its reputation. What regulators now require, and what these assets are ... Read whitepaper Article When AI Is Standard, Where Is the Edge in Drug Development? As AI becomes standard in drug development, where does competitive advantage lie? We examine clinical trial efficiency, asset selection, and ... Read article
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Whitepapers

news and resources
Whitepapers

Paz Sanz-Magallon Duque de Estrada, Consultant Intern, and Saadia Basharat, PhD, Senior Consultant

Recent Posts

Exosome & Extracellular Vesical-Based Therapeutics & Their Potential Use in Oncology

12th November 2021

Abstract It was previously believed that exosomes, membrane-bound extracellular vesicles released by cells, were a waste disposal mechanism resulting from cell damage or from by-products of cell...

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