OPERATIONAL HUBS: KOLKATABANGALORE
End-to-End Biotech Data

Solving Data Inadequacy
in Biomedicine.

Secure Assets for the Entire R&D Lifecycle.

We deliver EMR, Pathological, and Multi-omics data needed for every stage of research—from discovery to external validation. Powered by high-throughput AI agents and real-world hospital networks.

VIEW STAGES
Asset Infrastructure
ONLINE
20+
Linked Databases
Omics
Big Data Scale
AI Agents
High-Throughput
5+
Real-World Cohorts
10+
Diseases Covered
Multimodal
Data Capture
ISO COMPLIANT DE-IDENTIFIED & SECURE
Stage 01

Hypothesis
Generation

  • Novel biomarker identification via large-scale mining.
  • Target selection using multi-omics integration.
Stage 02

Discovery
Research

  • Mechanism of action studies on human data.
  • Patient stratification and phenotype clustering.
Stage 03

Pre-Clinical
Validation

  • In-silico validation against historical cohorts.
  • Retrospective correlation with clinical outcomes.
Stage 04

External
Validation

  • Testing models on independent hospital datasets.
  • Generating Real-World Evidence (RWE) packages.
Stage 05

Clinical
Translation

  • Bio-specimen collection for trial recruitment.
  • Regulatory submission data support.
Our Methodology

Complete Data Coverage

We bridge the gap between initial data mining and final clinical applicability through two integrated engines.

High-Throughput Discovery

Hypothesis & Discovery

Our in-house AI agents coordinate data delivery from over 20+ databases. We aggregate vast amounts of EMR, pathological, and big multi-omics data to fuel your initial hypothesis generation and discovery research.

  • Automated Data Aggregation
  • Multi-Omics Integration
  • Secure & De-identified

Real-World Validation

Translation & Validation

For pre-clinical and external validation, we utilize our active hospital network with 5+ established cohorts. We generate "real-world" datasets and fresh bio-specimens to prove your findings in a clinical setting.

  • Independent Clinical Validation
  • ISO Compliant Protocols
  • Recallable Patient Cohorts

Available Data Assets

From EMR to Big Multi-Omics.

REQUEST FULL CATALOG
STAGE: TRANSLATION

Metabolic Multi-Omics

Deep EMR linked with lipidomics and genomics for NAFLD/NASH progression.

Size 1,200+ Subjects
Type Real-World Data
STAGE: DISCOVERY

CVD Pathological Data

Resistant Hypertension cohort with longitudinal pathological records and serum data.

Size 850+ Subjects
Type Pathology/EMR
STAGE: VALIDATION

Solid Tumor Cohort

Paired pre/post treatment samples for external validation of oncology targets.

Size 3 Hospital Sites
Type Clinical Validation
STAGE: DISCOVERY

Breast Cancer Transcriptomics

Comprehensive sequencing data covering diverse molecular subtypes.

Sequenced 6,000+ Tumors
Cohorts 200+ Clinical
STAGE: VALIDATION

Solid Cancer Survival

Transcriptomic profiles linked with Overall Survival (OS) & Recurrence-Free Survival (RFS).

Patients 10,000+ Profiles
Data OS & RFS
STAGE: DISCOVERY

Spatial Imaging Data

High-resolution spatial analysis of breast cancer tumor microenvironment.

Sample 2,000+ Tumors
Format FFPE

Value Exchange

Supporting partners across the R&D workflow.

Pharma & Biotech

Discovery & Validation

Access "Real-world" datasets for external validation. De-risk your pipeline by testing hypotheses against ISO-compliant multi-omics data before Phase I.

Hospital Network

Data Source

Join our network of 5+ established cohorts. We deploy AI agents to structure your EMR data, turning patient volume into scientific value.

Academic Research

Hypothesis Generation

Leverage our high-throughput AI delivery from 20+ databases to generate robust hypotheses and accelerate publication timelines.

Compliance

Built on Trust.

We operate within a rigorous ethical framework. We ensure that data generation respects patient privacy while maximizing utility for discovery.

Verified
Encrypted

Ethical Clearance

All data collection is strictly approved by institutional review boards (IRB/IEC). We maintain auditable trails of consent and ethical approval for every dataset in our library.

Global Standards

Fully compliant with major data protection regulations ensuring seamless cross-border collaboration.

GDPR (UK/EU) HIPAA DPDP

Request Data Assets

Specify your R&D stage and data requirements. We will query our AI agents and hospital network.

01

Researcher Details

02

Data Requirements

Secure Submission (ISO)

Request Received.

Thank you for contacting QuantBioMed. We have received your query and our team will check the database availability. You will hear from us shortly.