

Clinical Trial / Protocol Statistics: DynaStat can help you with protocol
design and the statistical methodology to appropriately analyze the endpoints of your
clinical trial. DynaStat can provide you with the sample size calculations and Statistical
Analysis Plans to complete the statistical aspects of you protocol and submission.
DynaStat has experience in all phases of drug and medical device development, including
Phase IIIb, Phase IV, and REMS.
DynaStat is current on statistical methodologies such as adaptive designs and Bayesian
Statistics that allow you to more efficiently utilize your resources.
DynaStat also can provide the statistical programming to produce your tables, listings, and
figures to meet the requirements of the clinical study reports.
Meta Analysis: DynaStat has extensive experience in designing and performing meta
analyses from literature results and multiple clinical trials.
Sampling: DynaStat has experience in quality control sampling and audit sampling.
DynaStat can help you design a quality program for your manufacturing processes using
six sigma methodology.
Instruction: DynaStat can provide on site or off site statistical training for your clinical
staff including CRA, data management, and medical/clinical professionals. The unique
combination of industry experience combined with many years in a University allows for a
dynamic instruction process.
Novel Methodologies: Because of the diverse experience in the pharmaceutical
industry with large companies and small venture funded companies, DynaStat has
developed a propensity for independent thinking and offering different solutions to your
clinical trial development plan.
Statistical Consulting
DynaStat
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