Jeeva Exhibits at the NIH Rare Disease Day 2023
#RDDNIH we are exhibiting today and presenting poster at @NIH.
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Removing Socioeconomic Barriers and Increasing Diversity in Clinical Trials Would Have a Positive Economic Impact
Between logistical burdens, distrust in the healthcare system, and lack of awareness and information in many non-English languages, key demographic groups like women, children, low-income households, and racial and ethnic minorities are effectively left out […]
Jeeva Is Pleased To Be Featured In The Everest Group’s “Decentralized Clinical Trial Platforms PEAK Matrix® Assessment 2023
@Jeevatrials is pleased to be featured in the @EverestGroup ‘s Decentralized Clinical Trial Platforms PEAK Matrix® Assessment 2023. This rating shows that patient site experience is not an afterthought but rather runs parallel to the clinical […]
Jeeva TRIALMAGNET™ to Accelerate Study Recruitment And Retention
Patient recruitment is a major barrier in clinical trials. This involves the identification of patients, screening them for inclusion/exclusion criteria of a given clinical trial, and enrolling eligible patients into the trial. An all-in-one digital platform […]
2nd Annual Pharma Innovation Tech Congress 2022 – Virtue Insight
@Jeevatrials are delighted to be #Sponsor at the 2nd Annual Pharma Innovation Conference by Virtue Insight on 9th Nov’22, in Mumbai, India. Dr. @Harsharajasimha , the founder & CEO of Jeeva, will be present at the […]
Best of Times – Dr. Harsha Rajasimha & Jeeva Informatics
By adopting a checklist of key features or metrics that matter for your particular study, you can select a flexible software solution that best fits your clinical research needs. Then, you’re off to the races, track study progress, create data summaries, and prepare for regulatory compliance audits—all in one place. Following the 5 steps noted to overcome common research pitfalls can maximize the probability of success, save about 70% burden (hundreds of hours), and ensure great user experience in your clinical study.
New Jeeva eClinical Research Technology Enables Global Diversity Inclusion and Multi-Center Collaboration
By adopting a checklist of key features or metrics that matter for your particular study, you can select a flexible software solution that best fits your clinical research needs. Then, you’re off to the races, track study progress, create data summaries, and prepare for regulatory compliance audits—all in one place. Following the 5 steps noted to overcome common research pitfalls can maximize the probability of success, save about 70% burden (hundreds of hours), and ensure great user experience in your clinical study.
Technology Being Challenged by Upsurge in Decentralized Clinical Trials
As new non-COVID-related clinical trials proliferate, the need for effective global decentralized CT management is becoming even more apparent. What is needed, says Dr. Harsha Rajasimha of Jeeva Informatics, is to expand the capabilities of validated […]