ACT

march 27/2018


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news roundup

Worldwide Clinical Trials Acquires Late Stage Research Practice

Worldwide Clinical Trials, Inc. announced that the company has signed an agreement to acquire the Late Stage research practice of Continuum Clinical, LLC. This acquisition will expand Worldwide's ability to help life sciences industry sponsors establish evidence at each stage of the product life cycle.


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Where Expertise Meets Nuance: Conducting PTSD Clinical Trials
Live Webcast: Tuesday, April 24 at 11:00am EDT
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Certara Launches Quantitative Systems Pharmacology Consortium on Immuno-oncology

Certara announced the launch of its Quantitative Systems Pharmacology (QSP) Immuno-oncology Simulator Consortium. This new QSP brings together biopharmaceutical companies to create a simulator that can model clinical populations of cancer patients in order to improve the development of immuno-oncology therapies.


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Move Your Immuno-Oncology Therapy Forward in 2018 and Beyond
Live Webcast: Thursday, April 5 at 11:00am EDT
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Europe Adds More Voices to Orphan Drug Push

Rare disease interests in Europe add more voices to push for greater backing of research incentives, infrastructure.


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Scientific Advice with Regulators – An Essential Tool in Early Drug Development
Live Webcast- Europe: Thursday, March 29, 2018 at 3:00pm CEST, North America: Tuesday, April 17 at 11:00am EDT
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PAREXEL Introduces Medical Writing Solutions

PAREXEL International Corporation introduced PAREXEL's Medical Writing Solutions, a new offering that provides several communication services needed throughout each critical stage of the drug development and commercialization process.

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Patient-Centric Complex Trial Design & Site-Less Visits: How Study Design & IRT Can Ease Patient Burdens
Live Webcast: Wednesday, March 28 at 11:00am EDT
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In this edition

Europe Adds More Voices to Orphan Drug Push
Optimal Strategies for Compliance with EMA Policy 0070 on the External Publication of Clinical Data
Clinical Trial Educational Initiatives Can Improve
RBM—An Update of Experiences Among European CRAs

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Managing the Placebo Problem in Chronic Pain Studies
Live Webcast: Tuesday, March 27 at 11:00am EDT
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Events

Optimization of Cell and Gene Therapy Production
Expanded Access Programs 2018
Bridging Clinical Research & Clinical Healthcare Conference
IRT Europe 2018 - Interactive Response Technologies in Clinical Trials
Search Upcoming Events

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PV Research Reveals Momentum Towards Cloud and AL
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Articles

Optimal Strategies for Compliance with EMA Policy 0070 on the External Publication of Clinical Data

With the EU's new General Data Protection Regulation coming into force in May this year, the impetus for life sciences firms to cement their data management strategies has increased.


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The Benefits of a Data-driven Approach to Feasibility
On Demand
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Millennials and their Impact on Clinical Research

The importance of examining this generation's influence on the clinical trial value chain.

Blog Posts

Clinical Trial Educational Initiatives Can Improve

This article will analyze industry clinical trial initiatives and investigate strategies on how to improve impact on people.


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Achieve Better Early Clinical Development Outcomes - Faster
Use existing global network site relationships for improved early phase quality, costs and timelines
On Demand
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Buy a Diploma, Buy a Degree, Go to Jail

Education falsification has more consequences than not having a degree.


RBM

RBM—An Update of Experiences Among European CRAs

An RBM survey conducted in 2014 was repeated in 2016 in order to find out, how knowledge and practical experience with RBM have changed over that time period.


 

Adoption of RBQM in Academic Settings: Lessons Learned

This article discusses the adoption of RBQM in academic settings and the lessons that were learned.



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

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Todd Baker
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todd.baker@ubm.com