Advanced analytics solutions

Empowering Clinical Research with Innovative AI Solutions

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Who we are

Empowering Clinical Data Analytics with Innovative AI Solutions

Xpert Analytics specializes in Clinical Programming, Statistical Programming, Clinical Data Management and Data Analytics, providing cutting-edge AI-based content and code generation solutions. Our services cater to a wide range of clinical and regulatory needs, ensuring the highest standards of data management and compliance. Explore our offerings and discover how we can support your clinical development and operations.

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Our services

Transforming your data into actionable insights

Clinical Data Management

Data Collection & Cleaning: Streamlining data collection processes and ensuring data quality through automated cleaning techniques.
Database Design & Maintenance: Custom database solutions tailored to your clinical trial requirements.

Clinical Programming

SAS Programming: Expertise in SAS for creating, validating, and automating clinical trial data reports.
SDTM & ADaM Conversion: Efficiently converting raw data into CDISC-compliant SDTM and ADaM datasets.

Statistical Programming

Biostatistical Analysis: Comprehensive biostatistical analysis and reporting to support clinical trial outcomes.
R Programming: Utilizing R for advanced statistical modeling and analysis.

Clinical Operations

Project Management: Ensuring smooth execution of clinical trials with robust project management practices.
Monitoring & Reporting: Real-time monitoring and reporting to keep your clinical trials on track.

Regulatory Services

Regulatory Submissions: Preparing and managing submissions to regulatory bodies such as the FDA and EMA.
Compliance Consulting: Ensuring your clinical trials meet all regulatory requirements.

Clinical Science

Protocol Development: Crafting detailed clinical trial protocols to guide your research.
Medical Writing: Creating clear and concise documentation for clinical trial results and publications.

Pharmacokinetics

PK Modeling & Simulation: Advanced pharmacokinetic modeling and simulation to support drug development.
Bioavailability & Bioequivalence Studies: Conducting studies to determine drug absorption and equivalence.

Pharmacovigilance

Safety Data Management: Comprehensive safety data management to monitor and report adverse events.
Risk Management: Developing risk management plans to ensure patient safety and regulatory compliance.