12.06.22 -- Clinical Trials Enter A New Digital Era

The life sciences industry has been undergoing a transformation. It has seen advancements in how therapies are developed and improvements in how the industry works together. One development that has helped the industry evolve is the shift to digital technologies.

Discover why a unified CTMS platform is the answer for managing both the clinical trial itself and the data it produces when it comes to poorly integrated clinical trial management systems (CTMS).

First-generation eClinical systems can create as many challenges as they resolve. A more coherent solution is necessary to ensure data integrity, ease site burdens, and promote greater patient centricity.

The clinical research industry has been reluctant to adopt eConsent for several reasons, not least of which included having to disrupt already stressed and short-staffed work environments to implement new technologies. Read how the industry should continue exploring and implementing digital technologies in earnest.

As telehealth solutions and mobile health devices help empower decentralized clinical trials, discover how study sponsors are looking for ways to further improve the patient and site experience while delivering high-quality data.

EMR-to-EDC integration is challenging to scale due to the fragmentation of healthcare providers. With EMR interoperability, patients have the power to collect their own medical records and direct them into e-clinical platforms.

Explore why the implementation process for an eClinical supply chain management (eCSCM) platform needs to be collaborative and personalized to the individual clinical trial for each of the stakeholders.

This e-book focuses on the misconceptions around the cost-effectiveness of electronic patient-reported outcomes (ePRO) and also shares key points to consider when evaluating various ePRO solutions.

A must for all clinical leaders, this webinar shares strategic, operational, regulatory, and financial benefits of a seamless CTMS and eTMF integration. Watch the webinar to find out why CTMS-eTMF integration has increasingly become imperative for sponsors and CROs around the world.

Explore how Prancer RTSM utilizes natural language processing (NLP) and integrated supply forecasting to address the rising complexities and challenges of clinical trials.

Discover how Pro-ficiency's simulation training can better your clinical sites.

ISR’s CTMS Benchmarking & Market Dynamics (3rd Ed.) aims to tackle CTMS by helping providers and sponsors better understand current trends surrounding this technology and be able to anticipate future ones.

This video shows how a modern eTMF system built with a new exchange standard promises to bring better collaboration and compliance.

In this video, learn more about the full-service clinical trial management, virtual and hybrid sites, and comprehensive eClinical software platform that Curebase offers.

Accelerate and automate statistical analyses with the elluminate Statistical Computing Environment.

IQVIA Complete Consent combines a friendly, feature-rich technology platform that patients and sites are eager to use, with the powerful, scalable, operational infrastructure that sponsors need to make global implementations successful.