Dose Selection & Optimization Vendors

Compare partners for dose selection and optimization: quantitative justification of dose levels, regimens and adjustments for development and labeling.

Related workflows

Celerion is a CRO and laboratory services provider supporting clinical development, bioanalysis, biometrics, trial operations, and regulatory submissions.

Products: ClinQuick

Evidence-backed capability match
Matches Dose Selection & Optimization
“Study designs linking PK and PD endpoints provide essential data to make robust dose level decisions for later phase studies.”
Source: celerion.com

Also offers: First-in-Human (Phase I) Clinical Pharmacology Support, Clinical Trial Bioanalytical & Biomarker Testing, +2 more

Simulations Plus is a drug-development software and consulting provider offering PBPK modeling, pharmacometrics and QSP, and AI-driven drug design.

Products: GastroPlus, MonolixSuite +9 more

Evidence-backed capability match
Matches Dose Selection & Optimization
“For first-in-human studies, the next phase of development, pediatric dose selection, or for commercialization and labeling support, Simulations Plus uses a model-informed approach…”
Source: simulations-plus.com

Also offers: Model-Informed Drug Development (MIDD), PBPK Modeling, +3 more

Veristat is a specialty CRO providing biostatistics, clinical data management, and regulatory strategy and writing services.

Products: InStat, CoAuthor

Evidence-backed capability match
Matches Dose Selection & Optimization
“Selection of dose escalation and dose optimization design”
Source: veristat.com

Also offers: Biostatistics & Statistical Programming, Full-Service Clinical Trial Execution (CRO Services), +3 more

Althian Clinical Research is a boutique CRO supporting clinical trials, regulatory submissions, safety, data, and real-world studies in Mexico and LATAM.
Evidence-backed capability match
Matches Dose Selection & Optimization
“We support dose escalation studies to identify the maximum tolerated dose and establish safe therapeutic ranges. Our team uses stepwise escalation models and PK/PD data to guide…”
Source: althian.com

Also offers: Full-Service Clinical Trial Execution (CRO Services), Marketing Authorization & Lifecycle Submission Support, +3 more

ProductLife Group is a life sciences consulting and outsourcing group for regulatory affairs, pharmacovigilance, quality and validation, and market access.

Products: D.AI.M.I.

Evidence-backed capability match
Matches Dose Selection & Optimization
“First-in-human dose justification and Phase 2/3 trial simulations”
Source: plglifesciences.com

Also offers: Regulatory Development Strategy & Agency Interactions, End-to-End Pharmacovigilance Outsourcing, +6 more

Altasciences is an early phase CRO and CDMO providing toxicology, IND-enabling studies, clinical pharmacology, bioanalysis, and drug manufacturing.

Products: Acceleration Platform

Evidence-backed capability match
Matches Dose Selection & Optimization
“Dosing strategy: using ADME studies, we determine the appropriate starting dose for humans.”
Source: altasciences.com

Also offers: Toxicology Studies, First-in-Human (Phase I) Clinical Pharmacology Support, +2 more

IQVIA is a CRO and technology provider delivering clinical trials, real-world evidence, commercial intelligence and safety operations.

Products: IQVIA Vigilance Platform, SmartSolve +4 more

Evidence-backed capability match
Matches Dose Selection & Optimization
“When you need additional support in defining the optimal dose for latter phase trials, we can help through greatly improving the probability of success.”
Source: iqvia.com

Also offers: Full-Service Clinical Trial Execution (CRO Services), Real-World Data Platform, +6 more

Compare listed vendors

What this covers: Quantitative evaluation and justification of candidate dose levels, regimens, and adjustments for clinical development or labeling.

VendorDelivery modelAlso offersIn their words
AltasciencesCRO / Research Services ProviderExposure-Response Modeling, Bioavailability & Bioequivalence Studies“Dosing strategy: using ADME studies, we determine the appropriate starting dose for humans.”altasciences.com · reviewed Oct 21, 2026
Althian Clinical ResearchCRO / Research Services ProviderBioavailability & Bioequivalence Studies“We support dose escalation studies to identify the maximum tolerated dose and establish safe therapeutic ranges. Our team uses stepwise escalation models and…”althian.com · reviewed Oct 20, 2026
CelerionCRO / Research Services ProviderExposure-Response Modeling, Bioavailability & Bioequivalence Studies“Study designs linking PK and PD endpoints provide essential data to make robust dose level decisions for later phase studies.”celerion.com · reviewed Oct 12, 2026
IQVIACRO / Research Services Provider—“When you need additional support in defining the optimal dose for latter phase trials, we can help through greatly improving the probability of success.”iqvia.com · reviewed Oct 15, 2026
ProductLife GroupService ProviderExposure-Response Modeling“First-in-human dose justification and Phase 2/3 trial simulations”plglifesciences.com · reviewed Oct 26, 2026
Simulations PlusSoftware / Technology PlatformExposure-Response Modeling, Bioavailability & Bioequivalence Studies“For first-in-human studies, the next phase of development, pediatric dose selection, or for commercialization and labeling support, Simulations Plus uses a…”simulations-plus.com · reviewed Oct 26, 2026
VeristatCRO / Research Services Provider—“Selection of dose escalation and dose optimization design”veristat.com · reviewed Oct 26, 2026