Clinical Study Design & Software Development

Clinical Study Design & Software Development

Expert Statistical Planning for Clinical Research

Markov supports clinical research teams with statistical input and study-planning expertise across key stages of clinical study design.

Our capabilities include protocol statistical input, study design, endpoint definition, sample-size calculation, statistical methodology, randomization support and analysis population definition.

Our Clinical Study Design & Software Development

Protocol Statistical Input

Statistical input during protocol development to help align study objectives, endpoints and analysis requirements.

Study Design

Support in developing appropriate study designs based on the research objectives and clinical requirements.

Endpoint Definition

Support for defining relevant study endpoints and aligning them with the planned statistical methodology.

Sample Size Calculation

Statistical support for determining appropriate sample-size requirements for clinical studies.

Statistical Methodology

Selection and planning of appropriate statistical methodologies according to study objectives and analysis requirements.

Frequently Asked Question

Our study-design support includes protocol statistical input, study design, endpoint definition, sample-size calculation and statistical methodology.
Yes. Sample-size calculation is specifically included within Markov’s Study Design & Statistical Planning capabilities.
Yes. Randomization support is included as part of the study-design capabilities.

Explore Our Clinical & Software Solutions

From clinical study planning and protocol design to custom software development, we help transform complex research requirements into efficient, scalable, and technology-driven solutions.