Jeeva Exhibits at the NIH Rare Disease Day 2023
#RDDNIH we are exhibiting today and presenting poster at @NIH .
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The Benefits and Limitations of Clinical Data Platforms
The Benefits and Limitations of Clinical Data Platforms | By @MichaelCPace PhD | @Clin_Trials New opportunities for managing and designing #clinicaltrials have emerged, thanks to innovation in feasibility tools and data platforms.
Indian Society for Clinical Research Conference 2023
Our Founder & CEO, Dr. @Harsharajasimha is in India ! He will be speaking at the Indian Society for Clinical Research (@iscrindia) Conference in New Delhi on Feb 23rd & 24th, 2023. Reach out on LinkedIn […]
According to @BioBuzzMaryland, an assessment has been performed
According to @BioBuzzMaryland, an assessment has been performed by The American College of Clinical Pharmacology (@ACCP1_org ), a Virginia-based professional association of pharmacologists, that advances the calls for clinical trial diversity.
Dr. Harsharajasimha Interview With WTVM
Dr. @Harsharajasimha, the founder and CEO of @Jeevatrials, is interviewed by @IAMDeeArmstrong of @WTVM on how to help people understand the importance of clinical trials & perceive them from a different perspective. Video Link
The Rare Disease Diversity Coalition Webinar
Get inside Wall Street with StreetInsider Premium. Claim your 1-week free trial here. NOTE TO REPORTERS AND EDITORS: Members of the media and public are invited to a webinar on Tuesday, December 13 at 1:00 p.m. […]
Accelerate Conference 2022
Tue, November 1, 2022 at 12:37 PM-6 min read Accelerate Conference It’s an exciting moment for @Jeevatrials and its team because we will be presenting at the Accelerate Conference 2022 on Thursday, 3rd November 2022
Eye on the Community – The importance of ePROMs to supplement clinical assessments
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.
Empowering sponsors with compliant data collection and integrity for a variety of clinical studies
Traditional clinical guidelines, and stand-alone patient study and care pathways are proven to be increasingly inadequate, especially in a post-pandemic world with low clinical adherence, disrupted workflows, and stay-at-home orders. Disrupted workflows means more time required to […]
Dealing with challenges in quality evidence generation with a real-time analytical framework that makes clinical sense for innovators
Evidence linking interventions with health outcomes is vital for healthcare decision-making. Making sound choices about healthcare requires the best possible and quality evidence from clinical research. However, some of the decisions currently made during the drug […]