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PUBLICATIONS

European Pharmaceutical Contractor

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Spring 2017

   
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Data Management & IT Solutions
Spotlight

Transforming Software


Bracket’s Steve Rawbone and Stephane Deleger highlight the advantages of iterative design and user acceptance testing, detailing how this can reduce the complexity of clinical trials.
 
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DATA MANAGEMENT
Electronic Data Interchange

Destination: Automation


A hands-off approach to trials, through to the automation of processes such as the managing of inventories, is a new industry goal, but Ian Davison at HMD Clinical suggests that this raises its own questions.
 
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Supply Chain Management
Supply Management
 
Getting Interactive


Utilisation of intelligent IRT systems is the best way to meet the demands of clinical supply management, argues Stefan Dürr at Cenduit, as this can save time and eliminate unnecessary work.
 
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Local Trial Supply

The Hungarian Way


Many countries in the CEE region are now looking to local companies for several supply activities, so Tibor Kovacs at PharmaRoad expands on the reasons why Hungary is leading this trend.
 
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Managing Risk

Risky Business


Nils Markmann at World Courier explains how manufacturers can prepare for growing challenges in the modern mobile supply chain, protecting both themselves and patients.
 
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Published quarterly in
February, May,
August, and November

News and Press Releases

PCI Pharma Services Announces Organization Updates

Philadelphia, PA – May 20, 2019 – PCI Pharma Services, a leading biopharmaceutical outsourcing services provider, is pleased to announce the following management updates to help drive the company’s future vision, strategy and growth.
More info >>

White Papers

The Promise and Challenge of Adaptive Design in Oncology Trials

Medpace

Clinical oncology trials are more complex and time consuming than those in any other therapeutic area and failure rates are frustratingly high. Given the urgent need for new oncologic therapies, sponsors are eager to find more effective ways to conduct clinical research. Incorporating adaptive design methodologies into clinical trials can reduce costs and enhance efficiency while maintaining trial integrity. They can also reduce the number of patients on placebo and sub-therapeutic doses. In light of this promise, regulatory bodies have created guidelines supportive of adaptive design.
More info >>

Industry Events

PDA Europe Annual Meeting 2019

24 June 2019, Hilton Amsterdam

Featuring updates from international regulatory agencies as well as industry, this promises to become another highlight in the 2019 event calendar and is a meeting not to be missed!
More info >>

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