AI-Powered Drug Discovery & Development
Where Science Meets Intelligent Innovation
Our R&D Solutions Portfolio
We empower global pharma with advanced R&D solutions, enhancing drug discovery, clinical operations, regulatory compliance, and documentation through AI-driven automation. Achieve faster, precise results across all stages of development.
Drug Discovery & Preclinical Research
Clinical Operations Excellence
Regulatory Intelligence & Compliance
AI-Powered Documentation Suite
Drug Discovery & Preclinical Research
Empowering faster, data-driven drug discovery with AI-driven analytics and automation for preclinical research. Streamline candidate identification, enhance data precision, and reduce R&D timelines with tailored insights and solutions.
We offer:
Knowledge Extraction and Literature Search
Document Authorization
Knowledge Graphs
Impact: 80% automation in biomedical data curation with 90%+ accuracy
Clinical Operations Excellence
Enhancing clinical operations with AI-powered insights and automation to accelerate trials, optimize site management, and improve data accuracy. Streamline workflows and boost compliance to drive faster, cost-effective clinical outcomes.
We offer:
Clinical trial data enrichment
Document Authoring and standardization
Trial monitoring analytics
Impact: 20% improvement in clinical trial data verification across 20+ countries
Regulatory Intelligence & Compliance
Achieve seamless regulatory compliance with advanced AI solutions for real-time monitoring, data anonymization, and document automation. Streamline regulatory workflows, ensure accuracy, and stay ahead in the evolving compliance landscape.
We offer:
Automated regulatory documentation authoring and review
Compliance monitoring
Clinical document archival
Impact: 60% faster domain content generation for regulatory reports
AI-Powered Documentation Suite
Revolutionize documentation with AI-powered automation for faster, error-free data processing, conversion, and insights extraction. Streamline regulatory submissions, ensure compliance, and enhance document accuracy across the R&D lifecycle.
We offer:
Structured content authoring for clinical documents
GenAI for regulatory letter generation
Document process transformation
Impact: Reduced documentation time by 60% while maintaining accuracy
Our Impact in Numbers
1M+ PubMed Articles analyzed annually
36K clinical trials data points enriched
100K biomedical concepts indexed
10M clinical and regulatory data points processed
Our Capabilities
Powered by Custom AI Algorithms + Domain Expertise
600+ Life Science Subject Matter Experts
38+ PhDs across therapeutic areas
Specialized SMEs in clinical research and regulatory affairs
Our R&D Expertise
Data Asset Enrichment
Clinical data enrichment (structured/unstructured)
Risk assessment analytics
Biomedical concept indexing
Advanced text and image AI processing
Privacy & Compliance
Patient data protection
Regulatory-compliant synthetic data generation
Secure clinical data management
Global compliance standards adherence
Content Intelligence
AI-powered document generation
Clinical report automation
Regulatory submission preparation
Scientific content analysis
AInonymization
Advanced Named Entity Recognition (NER) Models
Human-in-the-loop Design
Classification of Identifiers
Compliance Assurance
Key Opinion Leaders (KOL)
Accurate KOL Identification for Targeted Influence
In-Depth KOL Profiling for Personalized Engagement
Dynamic KOL Segmentation for Strategic Alignment
Real-Time KOL Monitoring and Updates
Featured Case Studies
Transforming MedTech Surveillance: Achieving 99% Accuracy in Adverse Event Detection with AI-Powered Risk Analytics
Our AI-driven solutions accelerate drug discovery by automating data analysis, improving candidate identification, and reducing R&D timelines with high-precision analytics, offering up to 80% automation in biomedical data curation.
We provide clinical trial data enrichment, document authoring, trial monitoring analytics, and more, helping streamline workflows and improve data accuracy, which leads to a 20% improvement in trial data verification across 20+ countries.
Our regulatory intelligence solutions include real-time monitoring, data anonymization, automated documentation, and compliance monitoring, ensuring seamless adherence to global regulatory standards.
Our AI-powered documentation suite enables faster, error-free data processing, achieving a 60% reduction in documentation time while maintaining high accuracy across the R&D lifecycle.
With over 600 life science experts, including 38+ PhDs in various therapeutic areas, our platform combines custom AI algorithms with extensive domain knowledge to deliver tailored R&D solutions across drug discovery, clinical operations, and regulatory affairs.
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