StatFinn’s Services and Solutions bring client’s the expert support and operational excellence that everyone needs when conducting Clinical Trials. With over 10 years of experience in the industry as a company, StatFinn approaches every study in a unique manner that enables us to offer personalized interactions, customized solutions and highest quality results that the clinical research industry requires.
You can learn more about a particular service by clicking on the corresponding button below.
Sample Size Calculations
Statistical Analysis Plan (SAP)
Design of eCRF
Edit Checks, UAT
Protocol Input/Writing/ Review
Data Listings/ Review External Data
Data Safety Monitoring Board involvement
Statistical Reporting and Analysis for CSR
Statistical Report, Input and review of CSR
StatFinn’s expert team gets involved early in the planning process in order to work with both clinical and scientific teams to ensure consistent, robust study design. Providing Sample Size Calculations, Evaluation of Objectives as well as statistical methods approach together with Protocol input and writing, adds confidence to your study design and consistency in your program objectives.
Whether involved at the Planning stage or joining our client’s teams at the startup phase, we leverage our experience and knowledge in the industry to provide Protocol Input/Review as well as Randomization planning and design to drive the objectives and purpose of the studies. Naturally, we also compose Statistical Analysis Plans that create the framework for the achievement of the objectives for superior analysis results.
Our early involvement in the study conduct supports our clients throughout the lifecycle of Clinical Development studies and programs. We support Interim Analysis by not only delivering data, but also providing the analysis. We offer assistance for Data Safety Monitoring Board Committees and act as Independent Statistical Support for the decision making process. Our capability for making informed decisions based on results is an integral part of our approach to research.
The completion of our clients’ studies is our priority. From the Statistical Analysis and Report, to contributions to the Final CSR, StatFinn provides the Analytical experience and team support, to deliver top line results fast and full reported results on-time. At StatFinn we actively seek The Right Way to Conclusions.
Our Services in Data Management are based on lean processes guided by our Quality Assurance, years of experience and the ever changing industry standards, innovations and methods of operations. With over 50 years of experience within out Data Management Team from backgrounds in Pharma and CROs, we bring our customers top quality service, the highest customer focus and a driven Data Management team that is an integral part of any clinical study.
We provide services and solutions from database design through conduct and to final closeout and reporting. StatFinn’s wide variety of clients makes it possible to provide customized solutions that match YOUR needs. Whether it’s designing a study and executing from start to finish, providing resources to your teams on your systems or helping manage study rescues and migrations – our Data Management Operations Team is always where you need them, when you need them without compromising quality or budgets.
Overview of our services in Data Management:
- Database and eCRF design
- Use of various Industry EDC systems to offer a variety of solutions with close partnerships to developers to offer customized, as well as Integrated solutions, cost-effectiveness and consistent service.
- Industry Standards and Regulatory Compliance & Recommendations guided Operations & Processes – i.e. SDTM, CDISC
- Medical Coding
- Paper CRF management (Hybrid & Legacy studies)
CoPE: Consulting, Planning, Execution Services for Early Stage Development
With our CoPE Solutions, StatFinn’s Operational Teams and Experts get involved with clients early on in their Clinical Development planning activities. We work within the team to plan the statistical aspects of the trial to ensure scientific quality of objectives, GCP compliant protocols of the highest quality at industry competitive prices.
We also contribute at these early stages to assist in creation of clear study outlines and objectives to communicate the “big picture” to other stakeholders to also help achieve financial investment, program funding or decision processes.
With our wide range of services in both Statistics and Data Management we are able to help complete conceptual ideas and turn them in to concrete study programs and plans in order to advance into Clinical Development stages. All of the services that we offer can be put together into a CoPE package that is right for you.
For more information on how CoPE can work for you, please contact us at email@example.com