Pinnacle 21
Our team of experts leverages Pinnacle 21 to validate datasets against CDISC standards, identifying and resolving data issues early in the submission process. We offer comprehensive support for dataset validation, compliance checks, and regulatory submission readiness. Our deep understanding of regulatory requirements and industry best practices ensures that your clinical trial data is accurate, consistent, and ready for submission to global regulatory authorities. Trust us to deliver precise and reliable Pinnacle 21 services that support your clinical development goals
What we do?
Our expertise ensures precise, reliable data that guides your product from early stages to post-approval
Data Quality Review
Enhance the quality of your clinical trial data. Our team uses Pinnacle 21 to perform rigorous data quality checks, identifying and resolving issues before they impact your submission process
Submission Readiness
Prepare your datasets for regulatory submission with confidence. We utilize Pinnacle 21 to conduct thorough dataset validations, ensuring they are submission-ready and meet all regulatory requirements
Validation Services
Reduce manual errors and increase efficiency with our automated validation services. We deploy Pinnacle 21’s powerful validation tools to streamline the data review process, ensuring accuracy and compliance
Comprehensive Data Audits
Conduct in-depth data audits to identify potential issues early. Our experts use Pinnacle 21 to perform comprehensive audits, providing detailed reports and actionable insights for data correction
Training and Support
Empower your team with Pinnacle 21 training and support. We offer tailored training sessions and ongoing support to ensure your staff can effectively use Pinnacle 21 for data validation and compliance
Custom Solutions
Develop customized Pinnacle 21 solutions tailored to your specific needs. Our experienced team can create bespoke workflows and validation rules to address unique challenges and enhance your data management processes
Our Differentiators
Our expertise ensures precise, reliable data that guides your product from early stages to post-approval
Comprehensive Compliance
With our deep understanding of regulatory requirements, we ensure your datasets are fully compliant with CDISC standards, reducing the likelihood of submission rejections
Customized Solutions
Benefit from our tailored Pinnacle 21 services, designed to meet the unique needs of your clinical trials, ensuring optimal data validation and standardization
Cross-Functional Collaboration
Our integrated approach ensures seamless collaboration between clinical operations, biostatistics, and data management teams, enhancing overall project efficiency
Efficiency Optimization
Our streamlined processes and automation expertise reduce time and resource expenditure, allowing for faster and more cost-effective clinical trial execution
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