Fast CSP

Solid-form risk intelligence in two weeks

Fast CSP is a low-friction entry point into computational solid-form analysis. Submit a molecular structure and receive a full risk assessment — no experimental work, no lengthy procurement, no synthesis required.

What it is

A rapid, structured entry into solid-form analysis

Fast CSP is a fixed-scope, fixed-timeline engagement that delivers the core intelligence of CHEMINA™ without the complexity of a full programme. It is designed for teams at any stage of development who need to understand their solid-form landscape quickly.

Unlike experimental screening, Fast CSP requires no lab access, no solvent libraries, and no prior polymorph work. The entire process runs computationally — making it accessible from day one of a development programme.

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Two-week turnaround

From molecular structure submission to full risk report — delivered in as little as fourteen days.

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Fixed scope and deliverables

A defined output every time — no ambiguity about what you'll receive or when.

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No experimental prerequisite

A molecular structure is all that's needed. No synthesis, no prior screening, no lab work required.

What You Provide

Minimal input. Maximum intelligence.

Fast CSP is designed to remove the barriers that delay solid-form analysis. The input requirements are intentionally minimal.

Required

Molecular structure

SMILES string, InChI, or structure file. No synthesis or crystallisation required.

Optional

Dev context

Programme stage, known experimental data, or specific risk areas to prioritise.

Optional

IP context

Known patents or filing timelines that should inform the solid-form analysis.

What You Receive

A complete risk assessment, ready to act on

Every Fast CSP engagement delivers the same structured output — designed to inform decisions, not generate more questions.

Full solid-form landscape

A ranked map of all predicted polymorphs, solvates, and co-crystals for your molecule — computationally exhaustive.

Primary

Polymorph risk flags

Each form assessed for stability, solubility impact, and regulatory relevance — ranked by development priority.

Included

Screening guidance

Prioritised recommendations for any experimental follow-up, focusing resource where it matters most.

Included

IP overview

Initial view of known solid-form patents to inform freedom-to-operate and exclusivity strategy.

Included

Expert debrief

Structured review session with the Biosimulytics team to walk through findings, answer questions, and align on next steps.

Included
Why teams use it

Early insight that changes how programmes are run

Fast CSP fits into any development timeline — and delivers the most value when used earliest.

Pre-candidate selection

Identify the optimal solid form before committing to a development candidate — avoid downstream surprises entirely.

IND preparation

Generate the solid-form characterisation data required by ICH Q6A ahead of your filing timeline.

Licensing and partnering

Strengthen your data package with a comprehensive solid-form risk assessment before entering due diligence.

IP protection

Map the full solid-form space to identify patentable forms and assess exposure to third-party patents.

Formulation planning

Understand which solid forms are accessible and stable before committing to a formulation strategy.

Late-stage de-risking

Resolve outstanding polymorph questions quickly and de-risk your programme before Phase II or III investment scales.

Ready to asess your molecule's solid-form landscape?

Whether you want a rapid Fast CSP or a conversation about your programme, we are happy to talk. No commitment required.