FORMULATION DEVELOPMENT

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Persist combines AI-driven automation with an integrated robotic lab to accelerate formulation toward your QTPP. We can also coordinate with external partners for downstream studies and regulatory support.

OUR PROCESS

Built for high-throughput and efficiency.

  1. Design with our AI suite

    Our AI selects the top 12 formulations to match your QTPP. It takes into account API properties, IID Limits, excipient compatibility, excipient bioactivity, nitrosamine management, and more.

  2. Preformulation

    We run a comprehensive suite of solid phase characterization and phys-chem tests.

  3. Robotics build and test AI-designed formulations

    Our robotic systems then build and test candidates overnight, turning idle lab time into continuous progress.

  4. Feed results back to the platform

    As new experimental data is generated, the AI learns from each outcome. It uses these insights to design the next set of formulations with greater precision.

  5. Repeat until QTPP is met

    Each cycle brings the formulation closer to the defined QTPP. Once the target is reached, we move the top candidates forward into animal studies.

THE PROBLEM

Why traditional formulation falls short.

Formulation is hard. With limited trial-and-error and specialized knowledge requirements, every experiment is slow, deliberate, and designed to minimize risk. Much of the critical knowledge remains held by individuals, making it difficult to transfer and scale efficiently.

Problem / 01

Slow iteration cycles

Traditional CRO workflows are sequential, slowing optimization and delaying decisions.

Problem / 02

Limited exploration

Teams often evaluate only a narrow set of conditions before making key decisions.

Problem / 03

High cost of early mistakes

Weak formulation strategy leads to rework, delays, and lower downstream confidence.

THE SOLUTION

AI-guided formulation. Robotic execution.

Our platform provides a formulation knowledge base that enables teams to learn from every observation they make. Our robotic lab augments this knowledge base with real experiments done in our lab.

Solution / 01

AI decision support

Our AI suite helps our formulators learn from legacy data.

Solution / 02

Robotic data generation

We augment our experiments with formulation data that comes from our automation.

Solution / 03

Self-optimizing lab

Data is constantly fed back into the platform, optimizing itself with each iteration.

DIRECT COMPARISON

Persist AI vs. Traditional CROs.

Swipe to view full table →

CriterionPersist AITraditional CROs
Preclinical formulation scopeIntegrated preformulation → formulation strategy → optimization in a single, iterative systemSequential workflows across preformulation, excipient screening, and formulation development
Experimental throughputIn-silico screening across solubility, stability, and excipient combinationsLimited by manual lab capacity and batch-based experimentation
Formulation decision-makingAI-guided experiment design using prior data, physicochemical properties, and formulation constraintsTrial-and-error iteration with limited data coverage
Bioavailability & PK optimizationDesigned early for bioavailability, release profile, and PK alignment with target product profile (QTPP)Often addressed late after initial formulations underperform in vivo
Speed to viable formulationWeeks to reach a PK-ready or in vivo–testable formulationMonths of iterative cycles to reach PK-enabling formulation
Cost to reach PK-ready formulationSignificantly reduced cost through experimentation and optimizationTypically $100K–$500K+ across iterative CRO studies

CAPABILITIES

Modalities & formulations.

Cross-compatibility between drug modalities and the formulation technologies our platform currently supports.

ModalityMicrospheresIn Situ DepotsAmorphous Solid DispersionsIV ParenteralsSEDDS
Small Molecules
Peptides
Antibodies & Proteins
Antisense Oligonucleotides

ANALYTICAL TOOLS

Instruments under one roof.

Our capabilities are continuously expanding as we integrate new analytical tools and automation workflows. If you don't see a specific method or formulation type listed, reach out — we may already support it or can rapidly develop it.

Analytical ToolMeasurementsFormulation TypeRobotic?
BrightfieldParticle size, polydispersitySolids, semisolids, liquidsYes
Scanning Electron MicroscopyParticle size, polydispersity, and morphologySolidsNo
Dynamic Light ScatteringNanoparticle size, polydispersitySolids, semisolids, liquidsYes
Transmission Electron MicroscopyParticle size, polydispersity, and morphologySolids, semisolidsNo
High Pressure Liquid Chromatography (HPLC)Drug content and concentration, impurities, stability, size, refraction, fluorescence, absorbanceSolids, semisolids, liquidsYes
SpectrophotometryDrug content and concentration, fluorescence, absorbanceSolids, semisolids, liquidsYes
Raman SpectrometryDrug content and concentration, impurities, stability, solvent concentrationLiquidsYes
Dissolution ApparatusDrug solubility, dissolutionSolids, semisolids, liquidsYes
Moisture analyzerMoisture contentSolidsOn the roadmap
ViscometerViscositySemisolids, liquidsYes
Dynamic Foam AnalyzerFoam size, content, stabilitySemisolids, liquidsYes
TurbidimeterTurbiditySemisolids, liquidsYes
X-Ray MicroCTParticle morphology, internal porositySolids, semisolidsNo
Single-angle light scatteringParticle aggregation, quantitation, sizingSolids, semisolids, liquidsYes
Polarized Light MicroscopyCrystallinity measurementsSolids, semisolidsYes

FAQ

Frequently asked.

Don't see your question? Get in touch.

We support preclinical and clinical formulation development including:

  • Preformulation
  • PK-enabling formulation development
  • Early stability and compatibility testing
  • GMP testing
  • Phase 1 oral liquid formulations
  • Drug product strategy for IND planning

We do not support clinical trials or late-stage development.

Persist AI is a preclinical formulation CRO, not a CDMO.

We do:

  • Early formulation development
  • Drug product strategy
  • Screening and optimization

We do not do:

  • Large scale manufacturing
  • Commercial scale-up

No. We do not perform drug discovery, medicinal chemistry, toxicology, or clinical trials. We focus strictly on formulation and drug product strategy after a candidate is identified.

We support:

  • Solubility and bioavailability optimization
  • Excipient compatibility screening
  • Delivery route selection (oral, IV, SC, IP)
  • Stability and early drug product strategy
  • Controlled and modified release design

We work with a wide range of systems, including:

  • Amorphous solid dispersions (ASDs)
  • SEDDS / lipid-based systems
  • Microspheres and in-situ depots
  • IV and parenteral formulations

We work across:

  • Small molecules
  • Antibodies and biologics
  • Peptides and protein therapeutics
  • Nucleic acid therapies

GET IN TOUCH

Let's discuss your formulation needs.

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