The Psychology of Cancer: Suicidal Ideation in Clinical Trials
This article will analyze factors that affect suicidal ideation from a clinical psychiatric pilot study.
Applying New Technology to Randomization, Cohort Management and Dosing in Multi-center Early Phase Trials
The drive to accelerate drug development has highlighted the benefit in using RTSM systems within early phase cohort trials.
IOM Maps Out Data Sharing Program for Clinical Trials
Investigators and sponsors of clinical trials will have to make more detailed data available following study completion, according to a new report from an Institute of Medicine expert panel.
A Comprehensive Approach to Accelerating Clinical Trial Enrollment
It is well documented that lengthy start-up at individual trial sites related to contracting and committee reviews contributes significantly to delays.
MedNet Solutions Announces Latest Release Of Its Award-Winning iMedNet eClinical Solution
Systemwide Enhancements Deliver Exceptional Configurability, Performance and Efficiency
MedNet Solutions Latest Version of eClinical Solution
MedNet Solutions has released the latest version of its iMedNet™ eClinical, its cloud-based technology platform.
Report from Almac Confirms ePRO Benefits Outweigh Paper-Based Alternative for Clinical Trials
Almac announced the results of a survey conducted by researchers at the Tufts Center for the Study of Drug Development.
Almac Releases ePRO Data
The Quality of Clinical Trials
This article is the first in a series of articles that will review the development and findings of the first scientific measurement of quality in clinical trials.
Novella Clinical Partners with Academia on CV Clinical Trials Services
Novella Clinical and the Cardiovascular Research Foundation announced a preferred provider collaboration.
Novella Clinical and the Cardiovascular Research Foundation Collaborate to Provide Comprehensive Clinical Trial Expertise
Small Not Always Beautiful
Professor Sirpa Leppä pointed to the increasing challenge of inducing trial sponsors to select Finland in recent article.
goBalto Announces Latest Release of goBalto Activate
Over half of top 30 pharma and world’s largest CROs now using Activate worldwide
goBalto Activate Latest Version Available
goBalto released its latest version of goBalto Activate.
Oracle, Proteus Address Patient Adherence Data
Oracle and Proteus have integrated Proteus Digital Health Feedback System with Oracle Health Sciences InForm.
Oracle and Proteus Integrate Proteus Digital Health Feedback System with Oracle Health Sciences InForm to Help Increase Clinical Trial Accuracy
Oracle Health Sciences InForm electronic data capture platform utilizes Proteus solution, enabling greater accuracy in measuring medication adherence during clinical trials.
RbM Guidance Document: Ten Burning Questions about Risk-Based Study Management
This guidance document will offer information about RbM strategies.
Bristol-Myers Squibb Commits to Global Impact Partnership and Site Advocacy Group
INC Research First CRO to Launch Site Advocacy Group to Enhance the Clinical Research Process
Record Number of Medicines for Rare Diseases Recommended for Approval in 2014
Number of medicines with new active substances continues to increase.
Director General of EFPIA: “Pan-European HTA necessary”
Director General of EFPIA argued passionately in favour of the homogenization of European HTA bodies and regulation, during a recent interview
EFPIA Boss Renews Support for Health Technology Assessment
The Director General of EFPIA has spoken out strongly in favor of the homogenization of European health technology assessment bodies and regulation.
Qualcomm Announces Strategic Collaboration with Novartis to Optimize Global Clinical Trials
Novartis selects Qualcomm Life and its 2net technology to digitize its clinical trials
EMA Recommends Record Number of Medicines for Rare Diseases
In 2014, the European Medicines Agency (EMA) recommended the highest number of orphan designated medicines for marketing authorization in a year.
Novartis Selects Qualcomm Lifes 2net Tech to Digitize Clinical Trials
Qualcomm announced that its subsidiary, Qualcomm Life, has been selected by Novartis as a global digital health collaborator for its Trials of The Future program.
We Can Improve Oncology Trials Using Adaptive Designs
Today’s rich oncology pipeline-accounting for nearly 25% of agents in clinical development-promises much needed advances in cancer therapy.
Radiant Sage Releases RadClinica Version 3.0
Radiant Sage announced the release of its Clinical Trial Management System RadClinica™ version 3.0
Clinical Trial Management Solution Now Offers a Robust and Intuitive System with Real-time Information to Organize a Trial
Synchrogenix Acquires ClinGenuity
Certaa announced that its regulatory and medical consultancy, Synchrogenix, has acquired ClinGenuity.
Synchrogenix, Certara’s Regulatory and Medical Writing Consultancy, Acquires ClinGenuity
Deal provides Synchrogenix withproprietary technology, expert staff, and new capabilities to become the dominant player in life science regulatory and medical writing