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Bioavailability and Formulation Screening — Catalent

Catalent
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Scope with confidence. Review the published service details, then contact the CRO directly to confirm methods, timing, availability, and pricing.
Preclinical Research service category cover
Preclinical Research service category cover
  • Response Time
    Contact CRO
  • Delivery Time
    Project dependent
  • Location
    Somerset, NJ

About this service

The capability

At Catalent, we screen formulation and bioavailability-enabling approaches against the molecule’s developability risks.

A program-specific scope

We define the engagement around solubility, dissolution, permeability, solid state, API availability, target dose, route, modeling, and candidate technologies.

Expected outputs

Sponsors can expect comparative screening data, prototypes, development rationale, and a recommended path toward clinical supply.

When to engage us

This offering is intended for poorly soluble small molecules moving from late discovery toward formulation selection and Phase I.

Editorial note: Scope, availability, geography, and regulatory applicability should be confirmed directly with the provider. Official source reviewed: https://www.catalent.com/pharma/small-molecule/development/bioavailability-enhancement

Common questions

What can be included in screening and lead identification?

The proposed scope centers on screening workflows and data review supporting lead identification. Exact activities, methods, inputs, outputs, and responsibilities are confirmed with Catalent for the specific program.

Timing and pricing depend on project stage, complexity, required methods, available inputs, locations, quality requirements, and deliverables. Request a quote from the CRO after sharing a non-confidential project outline.

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