Statistical Analysis Solutions

Turn data into knowledge with our Data Analysis Solutions

Our Services

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Statistical Analysis Plan
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Our team of expert statisticians will work with you to develop a comprehensive and customised Statistical Analysis Plan for your clinical trial or RWE study. The SAP will outline the statistical methods and models that will be used to analyse the data, as well as the assumptions and limitations of the analysis. The SAP will ensure that the analysis is scientifically sound, ethically responsible, and compliant with regulatory requirements.

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Statistical Analysis Report
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Our team of expert statisticians will conduct a thorough and rigorous analysis of your clinical trial or RWE study data, using the methods and models outlined in the SAP. The results of the analysis will be presented in a clear and concise Statistical Analysis Report, which will include tables, figures, and interpretations of the findings. The SAR will provide a comprehensive and unbiased assessment of the safety and efficacy of the medical treatment being studied.

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Sample Size Calculation
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Our team of expert statisticians will work with you to determine the appropriate sample size for your clinical trial or RWE study. We will use statistical methods and models to calculate the number of participants required to detect a clinically meaningful treatment effect, while taking into account factors such as the expected variability in the data, the desired level of precision, and the planned analysis methods.

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CRF Development
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Our team of expert data managers will work with you to design and develop Case Report Forms (CRFs) that are tailored to your clinical trial or RWE study. The CRFs will be designed to capture the data required to address the study objectives, while ensuring that the data is accurate, complete, and compliant with regulatory requirements. The CRFs will be user-friendly and easy to complete, minimising the burden on study participants and investigators.

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Meta-analysis
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Our team of expert statisticians will conduct a meta-analysis of multiple clinical trials or RWE studies, using statistical methods and models to combine the results and draw valid conclusions about the safety and efficacy of medical treatments. The meta-analysis will provide a comprehensive and unbiased assessment of the available evidence, taking into account factors such as the quality of the studies, the consistency of the results, and the potential for publication bias.

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Survey (Inc. Delphi) Analytics
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Our team of expert statisticians will work with you to design and conduct surveys, including Delphi surveys, to gather data from experts or stakeholders. We will use statistical methods and models to analyse the survey data, identify patterns and trends, and draw valid conclusions. The survey analytics will provide insights into the opinions, attitudes, and beliefs of the survey participants, and will support decision-making and consensus-building.

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Why US

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SAP & SAR
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Therapy Areas
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Years of Cumulative Experience

Expertise and Experience

Our team of expert statisticians, data managers, and analysts have years of experience in the design, conduct, and analysis of clinical trials and RWE studies. We have the knowledge, skills, and expertise to deliver high-quality data analysis services.

Tailored solutions

We understand that every clinical trial and RWE study is unique, and we offer customised data analysis solutions tailored to your specific needs and objectives.

Quality and Accuracy

We are committed to delivering high-quality data analysis services that are accurate, reliable, and reproducible. We use rigorous quality control to ensure that the analysis is conducted in accordance with the study protocol and statistical analysis plan.

Timely Delivery

We use efficient and effective project management processes to ensure that the data analysis is conducted in a timely and cost-effective manner.

Collaborative Approach

We believe in a collaborative approach to data analysis, and we will work closely with you throughout the project to ensure that your needs and expectations are met.

Regulatory Compliance

We understand the importance of regulatory compliance in clinical trials and RWE studies, and we are committed to ensuring that our data analysis services meet all relevant regulatory requirements.

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FAQ

We offer a wide range of statistical analysis solutions, including study design, data management, statistical programming, and more.

Yes, our team can work with you to develop a comprehensive statistical analysis plan that aligns with your study objectives and timelines.

Yes, we can provide support for data visualization and reporting, including the development of tables, figures, and interactive dashboards.

Require a free consultation?

UK office: 86-90 Paul Street, London, EC2A 4NE.

Egypt office: 2 Hassan Shaker Street, Qism Damietta, Damietta First, Damietta Governorate 8040334.

UAE office: Block b-b36-194, Sharjah Research Technology and Innovation Park, University City - Sharjah

Quick links

MedDots Academy

Resources

Blogs

Solutions

Consensus Development

Publication Planning

MedCom

Scientific Event Support

Regulatory Writing

Digital and Multimedia Solutions

Statistical Analysis

AI Services

Contact

info@meddots.co.uk

Regional Offices

UK office: 86-90 Paul Street, London, EC2A 4NE.

Egypt office: 2 Hassan Shaker Street, Qism Damietta, Damietta First, Damietta Governorate 8040334.

UAE office: Block b-b36-194, Sharjah Research Technology and Innovation Park, University City - Sharjah

Quick links

MedDots Academy

Blogs

Resources

Solutions

Consensus Development

Publication Planning

MedCom

Scientific Event Support

Regulatory Writing

Digital and Multimedia Solutions

Statistical Analysis

AI Services

Contact

info@MedDots.co.uk

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