Biostatics
With 5 years of expertise, our biostatistics team delivers comprehensive support throughout the clinical development lifecycle. Our services include study design, data management, statistical analysis, and regulatory submissions. We ensure robust, reliable results, leveraging advanced methodologies and industry standards. Our tailored biostatistical solutions facilitate informed decision-making and streamline your product’s journey from early clinical development to post-approval. Partner with us for precise, insightful data that drives success in your clinical trials and beyond
What we do?
Our expertise ensures precise, reliable data that guides your product from early stages to post-approval
Study Design
We create robust study designs tailored to your research objectives, ensuring optimal data collection and statistical power to support your clinical hypotheses
Sample Size Calculation
Our team determines the appropriate sample size for your studies, balancing statistical precision with cost-effectiveness to ensure reliable and actionable results
Randomization and Blinding
We implement sophisticated randomization techniques and blinding processes to eliminate bias and enhance the validity of your clinical trial outcomes
Statistical Analysis Plans
We develop detailed statistical analysis plans (SAPs) that outline methodologies, endpoints, and data handling procedures, ensuring clarity and regulatory compliance
Data Management
Our data management services include database design, data cleaning, and validation, ensuring accuracy and integrity throughout the trial lifecycle
Post-Marketing Surveillance
We provide post-marketing biostatistical support to monitor product safety, efficacy, and market performance, ensuring ongoing compliance and product optimization
Our Differentiators
Our expertise ensures precise, reliable data that guides your product from early stages to post-approval
Customized Solutions
We offer tailored biostatistical services to meet the unique demands of your project, whether it's a small early-phase study or a large multinational trial, ensuring flexibility and precision in our approach
Integrated Data Management
Our seamless integration of data management and biostatistics ensures your data is clean, validated, and ready for analysis, reducing errors and enhancing the reliability of your results
Comprehensive Reporting
Our detailed and transparent statistical reports facilitate clear communication with stakeholders and regulatory bodies, ensuring all aspects of your study are meticulously documented and understood
Collaborative Approach
We work closely with your team, offering proactive consultation and support to ensure our biostatistical strategies align with your overall clinical development goals, fostering a collaborative environment for success
Our success based on how happy our clients are
As a full-service CRO, we specialize in clinical development, post-marketing,
and functional service support, ensuring your projects are managed with precision and integrity
Hira Technologies has been instrumental in the success of our clinical trials. Their expertise, responsiveness, and commitment to quality have kept our projects on track and within budget. Highly recommend for clinical development needs.”
Chief Medical Officer
Biopharma Company
Hira Technology’s post-marketing support has been crucial for our product’s success. Their proactive monitoring and detailed reports ensure compliance and inform our market strategy. Exceptional service and expertise.”
CRO
Pharma Company
Partnering with Hira Technologies for functional service support has streamlined our R&D operations. Their expert team integrates seamlessly with ours, delivering top-notch data management and biostatistics services. Outstanding professionalism.”
Head of R&D
Biotechnology Firm