Alchemy BioAlchemy Bio

The AI Biotech Operating
System

Turn complex biopharma workflows into automated AI pipelines, reducing manual effort and accelerating time-to-market.

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Autonomous Intelligence

Full Biopharma
Orchestration Layer

Autonomous Intelligence - Layered architecture visualization
Productivity Features

Turn months of work into days

Alchemy Bio automates biopharma workflows end-to-end — from preclinical research to compliance — lowering time costs, accelerating decisions, and eliminating the drag of repetitive processes.

Launch Planning, Market Access

Streamline indication assessments, KOL mapping, payer analyses, and launch readiness

Product Launch Tracker

Automate compliance, reduce submission risk

Track regulatory changes. Automate data coherence

Automate Compliance

AI Research Assistant

Scientist Copilots for all R&D Needs

AI Research Assistant

Accelerate Go To Market Enablement

Let AI build your GTM pharma strategy

Accelerate Go To Market
Biopharma Operating System - Workflow visualization
Key Capabilities

Smarter workflows,
built for biopharma

From commercialization strategy to regulatory compliance, Alchemy Bio equips teams with the tools to move faster, cut costs, and focus on high-value science

Structured for complex workflows
Accelerates time-to-market
Compliance-ready by design
Scales with your portfolio
Proof In The Numbers

Engineered for speed, savings,
and scale

Every workflow automated with Alchemy Bio translates into measurable leverage — saving time, reducing costs, and accelerating delivery across biopharma R&D and operation

Get Things Done

Cut timelines, reduce
risk, and unlock
leverage.

A full team of AI automation across all business units

Built with team logic
Adapts as work evolves
Insights without setup

Faster Trial Insights

AI aggregates patient data, publications, and registries into real-time dashboards — reducing protocol amendment delays and improving trial speed.

Patent & IP Safeguards

Instantly check drug candidates against global patent filings to flag risks and surface whitespace opportunities before heavy R&D investment.

Regulatory Gap Alerts

The system flags missing compliance modules or documents, ensuring submissions are complete and reducing the chance of costly rework.

Competitive Intelligence Feeds

Track competitor trial updates, publications, and partnerships automatically, delivered as concise intelligence briefings for decision-makers.

Portfolio-Wide Visibility

Connect research, regulatory, and commercial workflows into one view — making it easy to prioritize assets and allocate resources with confidence.

FAQ

Frequently Asked Questions

What makes Alchemy Bio different from other platforms?
Unlike generic AI or workflow tools, Alchemy Bio is built specifically for biopharma. We integrate R&D data, regulatory standards, and commercialization workflows into one operating system, automating the handoffs that normally cost months of delay.
Can this scale for larger teams or enterprises?
Yes, Alchemy Bio is designed to scale seamlessly from small teams to large enterprise organizations. Our platform supports role-based access controls, multi-team collaboration, and can handle the complexity of global biopharma operations.
Is the AI actually useful, or just a gimmick?
Our AI is purpose-built for biopharma workflows, trained on regulatory frameworks, and designed to augment your team's expertise—not replace it. It helps automate repetitive tasks, surface insights from your data, and accelerate decision-making with context-aware recommendations.
Is my data secure?
Absolutely. We maintain SOC 2 Type II compliance, use end-to-end encryption, and follow strict data governance protocols. Your proprietary research and regulatory data never leaves your control, and we never use customer data to train our models.
Can I customize workflows for different projects?
Yes, Alchemy Bio offers flexible workflow customization. You can create project-specific templates, define custom approval chains, and adapt processes to match your organization's unique requirements while maintaining regulatory compliance.

Request early access today!

Be among the first to cut your drug discovery timeline & cost in fraction.

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