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Home›Pharmacology›In Vitro-In Vivo Correlation
Process / pipelineBiopharmaceutics

In Vitro-In Vivo Correlation

In Vitro-In Vivo Correlation (IVIVC) · Also known as: IVIVC

IVIVC is a mathematical relationship between in vitro and in vivo properties of a drug, developed to predict oral bioavailability from dissolution data. Introduced by Amidon and colleagues in the 1995 Biopharmaceutics Classification System, it bridges laboratory measurements and clinical outcomes to streamline drug development.

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In Vitro-In Vivo Correlation
Dissolution f1/f2 Simila…Michaelis-Menten KineticsPhysiologically Based Ph…Arrhenius StabilityCaco-2 PermeabilityLiposome Encapsulation

When to use it

Use IVIVC when developing oral solid dosage forms to reduce reliance on clinical bioavailability studies. It is mandatory for biowaiver applications and most appropriate when dissolution is the rate-limiting step in absorption. Less useful if absorption is limited by permeability rather than dissolution.

Strengths & limitations

Strengths
  • Reduces cost and time for bioequivalence studies by predicting in vivo outcome from in vitro data
  • Enables formulation optimization without repeated human trials, supporting regulatory biowaivers
  • Provides early-stage decision support in development and post-approval manufacturing changes
  • Well-established regulatory framework (FDA, EMA guidance) with clear acceptance criteria
Limitations
  • Requires careful experimental design and sufficient variability in dissolution profiles to establish meaningful relationship
  • May not apply to drugs with complex absorption mechanisms (permeability-limited, fed-state sensitivity)
  • Level A correlations are difficult to establish; many methods achieve only Level B or C
  • Does not account for inherent drug properties (solubility, stability) outside dissolution scope

Frequently asked

What is the difference between Level A, B, and C IVIVC?

Level A is a point-to-point correlation with no averaging; it is the strongest and most predictive. Level B correlates mean in vitro dissolution with mean in vivo data. Level C is a single-point correlation (e.g., AUC to dissolution at 30 minutes). Level A and B require robust data; Level C is less rigorous but still acceptable for certain changes.

Can IVIVC replace clinical bioavailability studies entirely?

A strong Level A IVIVC can support a biowaiver to avoid repeat clinical studies for minor formulation changes. However, initial clinical studies are still required to establish the correlation. Once established and regulatory-approved, IVIVC can reduce or eliminate future trials.

What data do I need to build an IVIVC?

You need in vitro dissolution data (using USP apparatus with multiple time points) and corresponding in vivo PK data (AUC, Cmax from human or animal studies) for at least 3–4 formulations spanning a range of dissolution rates. More data points strengthen the model.

Why does IVIVC sometimes fail to predict outcomes?

IVIVC assumes dissolution is the rate-limiting step. If the drug is permeability-limited, food effects dominate, or pH variability in the GI tract is critical, the in vitro–in vivo relationship may not hold. Always verify the underlying assumptions.

Sources

  1. Amidon, G. L., Lennernäs, H., Shah, V. P., & Crison, J. R. (1995). A theoretical basis for a biopharmaceutic drug classification: the correlation of in vitro drug product dissolution and in vivo bioavailability. Pharmaceutical Research, 12(3), 413-420. DOI: 10.1023/A:1016212804288 ↗
  2. Shah, V. P., Amidon, G. L., & Levy, G. (1996). Level A, B, and C strategic approaches for biopharmaceutical classification-based dissolution specifications and in vitro-in vivo correlations. Pharmaceutical Research, 13(12), 1799-1801. link ↗

How to cite this page

ScholarGate. (2026, June 3). In Vitro-In Vivo Correlation (IVIVC). ScholarGate. https://scholargate.app/en/pharmacology/in-vitro-in-vivo-correlation

Related methods

Dissolution f1/f2 SimilarityMichaelis-Menten KineticsPhysiologically Based Pharmacokinetics

Which method?

Set this method beside its closest kin and read them side by side — the library lays the books on the table; the choice is yours.

  • Dissolution f1/f2 SimilarityPharmacology↔ compare
  • Michaelis-Menten KineticsPharmacology↔ compare
  • Physiologically Based PharmacokineticsPharmacology↔ compare
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Referenced by

Arrhenius StabilityCaco-2 PermeabilityDissolution f1/f2 SimilarityLiposome EncapsulationPhysiologically Based Pharmacokinetics

Similar methods

Dissolution f1/f2 SimilarityPhysiologically Based PharmacokineticsCaco-2 PermeabilitySolid DispersionPharmacokinetic Compartment ModelPopulation PharmacodynamicsArrhenius StabilityMichaelis-Menten Kinetics

Related reference concepts

Bioavailability and BioequivalenceAbsorption and BioavailabilityOral Administration and AbsorptionBiopharmaceutics and PharmacokineticsBioequivalence Studies and AssessmentRelative Bioavailability

Spotted an issue on this page? Report or suggest a fix →

ScholarGate — In Vitro-In Vivo Correlation (In Vitro-In Vivo Correlation (IVIVC)). Retrieved 2026-07-21 from https://scholargate.app/en/pharmacology/in-vitro-in-vivo-correlation · Dataset: https://doi.org/10.5281/zenodo.20539026
Quick facts
Originator
Gordon Amidon
Subfamily
Biopharmaceutics
Year
1995
Type
bioavailability prediction
Related methods
Dissolution f1/f2 SimilarityMichaelis-Menten KineticsPhysiologically Based Pharmacokinetics
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