ACT

AUGUST 20/2019


news roundup

IQVIA Launches Patient Portal

IQVIA has launched its IQVIA Patient Portal, available to trial participants upon trial recruitment. The portal guides the patients through the trial process with study visit and medication reminders, disease education, and concierge and travel support services, access to lab results, and upon trial completion, a plain language summary of the study, among other features. The Portal is part of IQVIA's full-service clinical trial offering or as a stand-alone solution.


Latest Business and People News

Read about the latest people and business news in the clinical trials industry.


Veeva's Vault Safety.AI

Veeva Systems has announced Veeva Vault Safety.AI, its new artificial intelligence (AI) application that automates case intake to reduce the time and effort of manual data entry for case processing. The application will be available April 2020.


Forte Announces Updates to its eRegulatory Solution

Forte has announced significant updates to its eReg solution, including multi-site regulatory management for both sponsors and sites and single-system essential document portfolio management capabilities across sponsored, IND/IDE held, and recruiting site clinical trials, among others.


Blog Posts

Addressing Patients Data Concerns

A new survey from Europe's leading rare disease organization, Eurordis, show a vast majority of the 2000+ rare disease patients responding to an international survey are supportive of data-sharing initiatives to foster research and improve healthcare, and willing to share their data to help research and treatment on diseases other than their own.


The Changing Needs of Mid-Sized Sponsors

Becky Carpenter, Head of North America/Euro Operations at WuXi Clinical, recently answered questions from Applied Clinical Trials about the evolution of the mid-sized pharma and CRO space.

In this edition

Latest Business and People News
Addressing Patients Data Concerns
The Changing Needs of Mid-Sized Sponsors

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Articles

Conducting Successful Pediatric Trials

There will continue to be a demand for pediatric trials that require large numbers of parents willing to enroll their children to participate in trials. Recruiting and supporting these young volunteers and their families requires a unique approach. Designing child-friendly protocols are essential to the success of your trial.

The Case for Responsive Adaptive Trial Designs for Rare Diseases

Adaptive designs are a promising option for rare disease trial sponsors, offering more control and better-informed decisions around progressing a drug through trial phases while improving patient outcomes, recruitment and retention.


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Lisa Henderson
Editor in Chief
LHenderson@mmhgroup.com

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Todd Baker
Group Publisher
TBaker@mmhgroup.com