DDi LLC software

COVID disruption and digitization acceleration made sponsors, sites and patients embrace technology like never before. Regulatory authorities’ attitude/approach and their comfort levels on “Data collection location - site vs home” changed as well. All these are positive signs for Clinical Research. mIRT platform helps speeding up deployment of studies. Users can reduce the risks, burdens, complexities, work-load, time and costs linked with managing all facets of global patient randomization and clinical trial supply management.

VISTAAR provides Global Regulatory, Clinical and Compliance Requirements to Biopharma, Devices, Consumer Health, Cosmetics, and Digital Health. With a unique combination of smart technology and subject experts, you will get up to date requirements and trusted insights accurately and much faster. Over many years, VISTAAR has built deep data sets to help you do the right strategy. All this is done at the best price point in the industry.