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International Clinical Trials

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Spring 2019

   
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End Point
End Point

Deadly Anti-Vaxxers

ICT’s Editor, Dr Graham Hughes, discusses the worrying increase in anti-vaxxers across the US and UK, highlighting the dangers of misinformation and unsubstantiated facts.
 
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Features
Q&A: Clinical Trials for Glioblastoma

Impatient Patients and a New Approach to Disease Treatment

Drawing from her own experience of glioblastoma, Jessica Morris at OurBrainBank talks to about the history of her company and her aim to empower patients by giving them back control of their own disease management.
 
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Successful Clinical Trial Execution and Oversight
 
Efficient and Effective Vendor Management

LUMIS International’sHeike Schön and Dr Fernando Martinez explain the urgency for effective vendor management relationships for small and midsize sponsors.
 
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Evaluating for Market

Achieving Successful Clinical Evaluation Reports

To assess the growing complications in clinical evaluation reports, Dr Efstathios Vassiliadis at Maetrics explores the history of medical device regulations and how to keep on top of a shifting regulatory landscape.
 
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Achieving Growth Potential in Clinical Research
 
The CRA Gap

Dietmar Eglhofer at VIARES evaluates the alarming shortage of experienced certified research analysts, which poses a threat to the clinical research industry and is detrimental to the growth potential of CROs.
 
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Patient Engagement
Evaluating Clinical Trial Satisfaction Rates

Busting the Patient Engagement Myth

BBK Worldwide’s Aaron Fleishman breaks down and challenges the commonly held beliefs about patient engagement and presents the opportunities ahead for clinical trial sponsors.
 
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Patient Perceptions

Interpreting Patient Reported Outcomes: A Holistic Approach

Health Outcomes InsightsDr Keith Meadows presents a new approach to interpreting data from patient reported outcomes and advises on how to compensate for imperfect data.
 
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Patient Engagement Technology in Clinical Trials

Enhancing the Patient Experience

New technological advances should be utilised by CROs and study sponsors to improve patient satisfaction and engagement, as discussed by James Munz and Chris Watson at ERT.
 
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Patient Participation in Clinical Trials

Receptivity, Recruitment, and Retention

To alleviate the inherent problems with patient engagement and recruitment, Christian Burns, Joan Chambers, and Melissa Daley at ClinX push for new ways to drive ‘the three Rs’: receptivity, recruitment, and retention.
 
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Implementing the Patient’s Voice in Clinical Trials

The Mosaic of Patient Engagement

Patient perspectives in clinical research are a significant talking point in the development of trial design technology. Worldwide Clinical TrialsBarbara Zupancic and Dr Michael Murphy explore the value in implementing these technologies.
 
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A Unified Approach to Patient Engagement
 
The Perverse Incentive

Matthew McCarty at ICON establishes a greater unified approach to patient engagement, retention, and compliance through patient-facing technologies.
 
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Therapeutic Focus: Oncology
Precision Medicine in Modern Day Oncology

The Patient Data Paradigm

Dr Aldo Poli at OPIS examines the use of precision medicine in treating cancer and the importance of approaching clinical research from the patient’s perspective.
 
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eClinical Technologies
Developing a Unified eClinical Platform

E Pluribus Unum: Out of Many, One

Oracle Health SciencesCraig Morgan addresses the numerous inefficiencies in organisational siloes and how consolidation technologies may be the answer.
 
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Q&A: The Role of Technology in Clinical Trial Logistics

Utilising Technology on a Global Scale

Kyle Cunningham at Greenphire speaks with ICT about the use of new technologies in combatting the burdens of clinical trial research and logistics.
 
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Clinical Trial Insurance
Making Clinical Trial Data Accessible to Patients

A Three-Pronged Strategy

Data transparency and disclosure are a vital talking point in the wider scope of clinical trial insurance. Thomas Wicks at Trialscope discusses options for more accessible data to patients on a local and global scale.
 
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Edited by
Dr Graham Hughes
Consultant in
Pharmaceutical
Development

Published quarterly in
February, May,
August, and November

News and Press Releases

WuXi STA and Dizal Pharmaceutical Sign CMC Development and Manufacturing Agreement

STA Pharmaceutical Co., Ltd., (WuXi STA) – a subsidiary of WuXi AppTec – and Dizal Pharmaceutical, a biotechnology company, announce a strategic partnership. Under the terms of the collaboration, WuXi STA will become the preferred CDMO partner of Dizal Pharmaceutical for GMP production, providing integrated CMC (Chemical, manufacturing and Control) process research and manufacturing services from API to drug product.
More info >>

White Papers

Soothing the Logistical Headache of Clinical Trials

Equilibrium Travel Management

As many as 30 per cent of subjects on phase three clinical studies drop out.  Gruelling schedules, high travel costs and time waiting for expense reimbursement can all be factors in these fall rates, and this can be very problematic, delaying or even leading to the cancellation of the trial.  It is crucial to keep subjects motivated, and through efficient travel and expense management, this can be achieved.
More info >>

Industry Events

The Universe of Pre-filled Syringes and Injection Devices

22-23 October 2019, The Swedish Exhibition & Congress Centre Gothia Towers Hotel

PDA’s Universe of Pre-filled Syringes and Injection Devices has become the must-attend meeting for everyone working in the field, and is now the world’s largest conference on this subject
More info >>

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