Transaction significantly expands CHS's ambulatory marketplace growing footprint and revenue cycle management services.

A Strategic, Technology-Driven Approach

C-suite, hospital boards and senior managers from 709 hospitals and inpatient organizations responded to a Q2 2018 outsourcing user survey.

Session will help practitioners understand the benefits of using the tool and how organizations can proactively manage receipt acknowledgements, oversee distribution from a user-friendly dashboard and increase overall compliance in a cost-effective way through automation

Sonder Health telehealth strategy consulting and clinical delivery services help organizations successfully implement telemedicine programs

Learn how eSource is reshaping the time and cost efficiencies of modern clinical trials

In a clinical research industry that prizes speed and cost efficiency above all else, the importance of preventing EDC database delays is difficult to overstate. But how can data managers ensure they're equipped with the tools and the know-how to do so?

New Black Book study shows rising customer expectations and lower satisfaction rates based on provider technology

Comprehensive Interrogation of the Genetic Determinants of Female and Male Infertility: A New NGS Research Application Enabled by Improvements in Target Enrichment Technology

This webinar will offer best practices for UAT for sponsor organizations with the aim of changing the conversations and expectations around the UAT process

Thirty percent of practices with over 11 clinicians expect to replace their current system by 2021 for customization issues

According to the 2017 Tufts eClinical Landscape Study, 97% of companies plan to increase use of at least one clinical data source over the next three years. But today, 98% of companies report challenges with their clinical data management systems.

Live interactive session will focus on how technology can help clinical trial leaders move the needs of the patient and the site to the center of the clinical trial

Duplicate and fragmented shared patient records are progressively putting patient safety at risk and afflict provider bottom lines.

Achieving Orphan Drug Designation is a significant step enabling your product to be licensed faster, in a cost-efficient manner, and achieve market exclusivity for 10 years.

The race is on for non-alcoholic steatohepatitis (NASH) drug development as the disease—which has no approved treatments—is rapidly growing in prevalence and is the fastest rising cause of liver transplantation in the United States.

Bring your own device (BYOD) solutions offer a disruptive alternative to the costly provisioned solutions for ePRO but have been mostly overlooked and only moderately considered due, in part, to this question of equivalence and to concerns for patients accepting study tools on their own phones.

Webinar describes how Agios Pharmaceuticals is solving business and data challenges by implementing a Clinical Data Hub including key selection criteria, implementation best practices, and lessons learned.

Patient engagement experts from Bracket and Boehringer-Ingelheim to discuss technology selection and implementation strategies for clinical trials.

Experts from Comprehend and Tufts CSDD to discuss the recent study, outline where the industry is headed and ways to overcome oversight challenges including transparency, risk, and compliance

BioMauris becomes only fifth company with a state-level cannabis contract

Integrated and Managed Best-in-Class Hardware & Software Platforms to drive Efficiency, Savings and Simplicity for Hospitals, Clinicians and Patients

Executives share groundbreaking research on the use of longitudinal patient information to improve quality reporting at HIMSS 2018

Presenters discuss how clinical innovators, Market Access, IT and HEOR can accelerate RWE initiatives and the implications for data security and healthcare decision-making