1.
Custom Statistical Analysis Plans (SAPs)
1.
Our experienced team of data scientists work in sync with your research goals, developing bespoke Statistical Analysis Plans (SAPs) for your clinical trials and Phase Studies. We strive to contribute our statistical acumen to every stage of the process, and actively engage in the review of SAPs, ensuring robust, reliable outcomes.
2.
Protocol Optimization and Review
2.
The bedrock of any clinical trial is a well-structured protocol. Our team's meticulous attention to detail ensures the statistical methods sections of protocols are developed to the highest standards, while our comprehensive review of Case Report Forms (CRFs) enhances data collection effectiveness, maximizing the value of your trials.
3.
Precision in Report Generation
3.
Clarity and accuracy in reporting are crucial in the pharmaceutical industry. Our team excels at crafting statistical sections of study reports, illuminating your findings with precision. We also extend our problem-solving prowess to tackle issues in study protocol or statistical analysis, safeguarding your research integrity.
4.
Clinical Data Management Redefined
4.
Navigating the sea of clinical data is a complex challenge, but one that Softqube is well-equipped to handle. Our advanced data management techniques bring clarity to complexity, unlocking the potential of your data and revealing insights that guide your research.
5.
Advanced Statistical Modeling
5.
Our team is proficient in a range of statistical modeling techniques, from sample size calculation and hypothesis testing to correlation and regression. Utilizing industry-leading statistical software packages like R, Minitab, and Python, we help you build predictive models that inform your research strategies.
6.
Integral Team Participation
6.
We believe in fostering a collaborative approach to clinical trials. Our team actively participates in clinical trial activities, particularly phase 2-4, integrating our statistical expertise with your cross-functional team’s strengths.
7.
Comprehensive Documentation
7.
We recognize the importance of comprehensive and accurate documentation in clinical research. Our team ensures every data issue, statistical method, and analysis result is meticulously documented and interpreted, creating a robust record of your research journey. We present results in easy-to-understand tabular and graphical formats, facilitating effective communication and decision-making.
8.
Reliable Internal Auditing
8.
Softqube champions quality assurance and regulatory compliance. As part of the internal audit team, we conduct rigorous audits of protocol, data, and reports, ensuring the highest quality and compliance standards are met.
9.
Experience the Softqube Difference
9.
Rely on Softqube Technologies for a new paradigm of data analytics in the world of CROs and Pharma companies. Embark on a journey with us and witness how the power of data, when harnessed by experts, can transform your research outcomes and expedite the path to groundbreaking discoveries.
