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European Pharmaceutical Contractor

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Winter 2019

   
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Clinical data
Precision Medicine Challenges

Realising International Data Access through Data Collaborations

Randy Ramin-Wright and Le Vin Chin at Clinerion explain how gaining access to real-world data on a global scale does not have to be intimidating and can be readily achieved through the use of the latest consolidation technologies.
 
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Data Oversight and Integrity

Improving Quality Using Centralised Statistical Monitoring

With new regulations and the continuing importance of quality management over regulatory submissions, monitoring data integrity and oversight is pivotal to success. Thomas Underwood at Quanticate explains more.
 
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CRO Consolidation and Global Growth

Exploring Growth Strategies for Smaller CROs

The life sciences industry is no stranger to mergers and acquisitions, particularly when discussing midsized CROs. Zac Beda at Upsilon Global examines the practice and looks into the benefits.
 
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Published quarterly in
February, May,
August, and November

News and Press Releases

Northway Biotechpharma Celebrates 15 Years of Growth and Success

Vilnius, Lithuania, July 16, 2019 ─ Northway Biotechpharma, a leading biopharmaceutical contract development and manufacturing organization (CDMO), celebrates its 15th anniversary today. As a midsized CDMO, Northway Biotechpharma is able to provide flexibility and responsiveness backed by a strong foundation in science and technology. The company focuses on understanding its customers and meeting their specific needs without binding them to one single approach. It is able to react rapidly to unexpected project changes, adjusting timelines, capacities and other activities to meet its customers’ evolving needs. On average, Northway Biotechpharma has 25–30 development projects underway each year, ranging from gene cloning to final drug product manufacturing.
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White Papers

Running Smarter Trials With Data-Driven Monitoring

PAREXEL

Clinical monitoring remains one of the most important and most costly activities in the clinical research paradigm.  Monitoring provides the operational transparency required by investigators, sponsors, and regulators to make informed decisions about site performance, patient safety, and overall study progress. Yet unlike many clinical trial activities, which have been steadily transformed by technology, the monitoring function itself has changed little.
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Industry Events

2020 Avoca Quality and Innovation Summit

3-4 June 2020, Amsterdam, The Netherlands

The 2020 Avoca Quality and Innovation Summit will take place 3-4 June 2020, in Amsterdam, The Netherlands.
More info >>

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