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QuantRX(R&D)

A powerful solution that streamlines pharmaceutical research and development with centralized data, regulatory compliance, and real-time project tracking.

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MOLECULE TO MARKET — AI THAT ACCELERATES DRUG DISCOVERY

QuantRx is an AI-powered platform that transforms the pharmaceutical R&D lifecycle — from drug discovery to post-market surveillance. It advanced analytics, machine learning, and realworld data to accelerate development, reduce costs,and improve success rates.

Drug Discovery
Omics Data Analysis

Integrates genomics, proteomics, and transcriptomics data

Knowledge Graphs

Maps complex biological relationships for novel target discovery.

Disease Association Modeling

Predicts gene-disease links using public databases

Virtual Screening

AI filters millions of compounds to identify promising candidates.

Docking Score Prediction

Deep learning models forecast binding affinities to targets.

QSAR Modeling

Quantitative structure-activity relationship models to refine leads.

Preclinical Development
ADME Prediction

Forecast absorption, distribution, metabolism, and excretion properties using predictive models.

Bioavailability Analysis

Simulate how candidate drugs behave in the human body without lab testing.

Toxicity Classifiers

Identify hepatotoxicity, cardiotoxicity, and other safety risks using trained models.

Early Risk Flagging

Detect potential adverse effects before animal studies, reducing costly failures.

Compound Testing

Simulate drug interactions in digital models of biological systems.

Data Aggregation

Centralizes lab, assay, and predictive data for real-time insights.

Clinical Development
Trial Frameworks

Enable dynamic protocol adjustments based on real-time data.

Historical Trial Analytics

Used AI to learn from past trial data andrefine inclusion/exclusion criteria.

EHR Mining

Extract eligibility criteria from unstructured clinical records

Stratification Tools

Identify subpopulations with higher response potential for targeted recruitment.

Risk-Based Monitoring (RBM)

Automatically prioritize sites and patients for closer oversight.

Patient Response Analytics

Used machine learning to monitor biomarkers, treatment efficacy, and safety signals during trials.

Formulation & Manufacturing
Physicochemical Stability

Forecast compound behavior over time under various conditions using machine learning.

Dosage Form

Recommend the best form (tablet,capsule, injectable) based on solubility,bioavailability, and patient profile.

Twin Simulations

Create virtual replicas of manufacturing processes to test changes without disrupting operations.

Process Control

Continuously optimize mixing, granulation, and drying steps for quality and efficiency.

Predictive Maintenance

Forecast equipment failures before they happen, minimizing downtime.

Post-Approval & Pharmacovigilance
Signal Detection

Automatically identify potential adverse drug reactions (ADRs) from large-scale real-world data.

Multi-Source Integration

Aggregate data from EHRs, claims, registries, and social media platforms

Predictive Risk Models

Anticipate safety concerns before they escalate using historical and real-time data.

Stratified Safety Analytics

Assess drug safety across diverse populations, geographies, and comorbidities.

Data Infrastructure & Governance
Unified Data Repository

Integrates data across drug discovery,clinical trials, manufacturing, and postmarket surveillance.

Multi-Type Data Handling

Supports structured (e.g., lab data,EHRs) and unstructured (e.g., clinicalnotes, sensor data) formats.

Real-Time Ingestion Pipelines

Continuous data flow from lab systems, EDCs, LIMS, and external sources.

Industry Standards Support

Natively supports CDISC, HL7, FHIR, and OMOP formats.

Request a call back

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Industries we covered
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Biotechnology
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Vaccines
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Dietary
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Veterinary
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API
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Nutraceuticals

AI Evolution in QuantRX

For target-disease association, clinical trial outcomes, ADME/Tox prediction, and patient responses.

Used in toxicity prediction (e.g., hepatotoxicity), regulatory risk detection, and adverse event categorization.

Stratify patients, compound clusters, and manufacturing process behaviors.

Design novel compounds using SMILES-based GANs and variational autoencoders (VAEs).

Auto-generate initial clinical trial protocols from historical benchmarks.

Things You Get


Our Expertise

Working with our certified experts means you get tailored, high-quality solutions, delivered on time and within budget. We ensure seamless collaboration, leveraging industry-best practices to bring your vision to life with efficiency and reliability.

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Product Consulting
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Customized Solution
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Scalable Solution
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User-friendly Interface
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Data Security
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Dedicated Support