ACT

OCTOBER 30/2018


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news roundup

PAREXEL and Datavant Partner to Deliver Data and Real-World Evidence Analytics

PAREXEL and Datavant, Inc., a healthcare technology company focused on enabling the secure de-identification and linking of healthcare datasets, announced they are partnering toward clinical study design and operations, as well as the generation of RWE. The collaboration hopes to enable the linking of healthcare data from a variety of real-world and clinical study data.

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How clean is your clinical trial data?
A large group of clinical data management professionals were surveyed and 58% were not confident in the quality and completeness of their clinical data from an audit/compliance perspective. This is a brand new, in-depth report on Challenges and Opportunities in Clinical Data Management, conducted by Pharma Intelligence and sponsored by Oracle Health Sciences.
Click here now to download the free survey report

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Partnerships in Clinical Trials Europe
27-29 November 2018
CCIB | Barcelona
Explore a world of clinical knowledge at this year's Partnerships in Clinical Trials Europe as the experts take to the stage to present the latest data and insights into how they're transforming clinical trials. From new patient focussed initiatives and strategic partnership advice through to AI and the new Clinical Trials Regulation, PCT Europe has it covered.
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In this edition

Global CRO Signs TrialOne Agreement With OmniComm Systems
Improved Understanding of Psoriasis Buoys Treatment Hopes for Patients
FDA Seeks Reliable Patient Information to Support Regulatory Decisions


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Aptus Clinical and the Cell and Gene Therapy Catapult Announce Their Clinical Service Partnership

CRO Aptus Clinical has been appointed as a supplier for clinical services by the Cell and Gene Therapy Catapult (CGTC). As an early-phase CRO, its role is to support development and delivery of advanced therapy studies in the UK and Europe. Through this partnership, Aptus Clinical will primarily provide dedicated site set-up and monitoring of investigational sites for the CGTC's collaborators.


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Early Clinical Development
27-29 November 2018
CCIB | Barcelona
Get to grips with the latest early phase clinical updates and insights at this year's Early Clinical Development meeting as leading experts delve into the new FiH guidance, patient engagement and recruitment strategies, clinical trial design, rare disease therapies, biologics, cell and gene therapies, and lots more, to help you tackle your biggest phase I and IIa challenges and fast-track your path to proof-of-concept.
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Clinerion and S4 Research Partner

Clinerion and S4 Research announce a partnership to expand the global network of hospitals on the Clinerion's Patient Network Explorer platform into India. S4 Research's wide network in India and clinical trials experience, will support Clinerion in the expansion of its global network of partner hospitals in India.


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The Potential for Disease-Modifying Therapies in Parkinson's Disease
Tuesday, November 13, 2018 at 11am EST|8am PST|4pm GMT|5pm CEST
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Global CRO Signs TrialOne Agreement With OmniComm Systems

A global CRO has signed a new agreement extending its relationship with OmniComm Systems, Inc., a provider of clinical data management technology, for another seven years. Under the terms of the agreement, the CRO will use OmniComm's TrialOne eClinical solution in order to automate early phase studies at one of its U.S.-based clinical research units.

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Cellular Biomarkers: Predicting Clinical Trial Outcomes Through the Understanding of T-cell Responses in the Human Challenge Model
North America: Tuesday, November 13, 2018 at 11am EDT | 10am CDT | 8am PDT
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Events

Women of Color in Pharma Second Annual Conference
2018 HBA Annual Conference
Independent Expert Committees
Pharmacovigilance Audits and Inspections Summit
Crossroads: An Artia Solutions Conference
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Cellular Biomarkers: Predicting Clinical Trial Outcomes Through the Understanding of T-cell Responses in the Human Challenge Model
Europe: Thursday, November 8, 2018 at 3pm GMT | 4pm CET
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Neuropathic Pain Studies: Patient Selection, Study Design, and Clinical Trial Challenges
Tuesday, November 6, 2018 at 11am EST | 8am PST | 4pm GMT | 5pm CET
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Articles

RBM: Barriers to Adoption

The results of a 2018 survey of sponsor, CRO, and technology companies.


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IDENTIFYING NASH PATIENTS: Solutions and Strategies
Thursday, November 1, 2018 at 11am EDT
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Improved Understanding of Psoriasis Buoys Treatment Hopes for Patients

Advances in our understanding of the genetic, immunological, and environmental factors that contribute to the pathogenesis of psoriasis have led to the development of very effective precision therapies that alleviate patient morbidity and improve quality of life, especially for patients with moderate to severe disease.


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On the brink of change: How academic data and machine learning can revolutionize Alzheimer's drug development
On Demand
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Blog Posts

FDA Seeks Reliable Patient Information to Support Regulatory Decisions

As FDA continues to advance the role of patients in designing clinical trials with meaningful and accurate endpoints, it is seeking more input from stakeholders on how best to identify clinical outcomes most important to patients and caregivers.


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Research Reveals Data Quality Issues Slow Clinical Trial Progression – What Can You Do To Prevent This?
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Quiz Time: What Methods Would You Use for HTA?

Imagine you are in charge of European legislation on pharmaceuticals. Imagine you've been told to draft rules on how to conduct clinical assessments at European level to help measure the value of a medicine. What would you go for?

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Lisa Henderson
Editor in Chief
Lisa.Henderson@ubm.com

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Todd Baker
Group Publisher
todd.baker@ubm.com