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European Pharmaceutical Contractor

epc
Winter 2015

   
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Marketplace & Business
CRO Growth

Deal Me In


Contract research continues to thrive as CROs strengthen their R&D services and sponsors tighten their budgets. Growth is surging this year and predicted to at least the end of the decade, driven by the big players and market consolidation. EPC has more.
 
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Legal & Regulatory
Patent Protection

Optional Extras


It is uncertain times for patent portfolios in Europe, with pharma companies large and small working out whether to opt in or out of the Unifi ed Patent Court system, coming in 2017. The risks, rewards and – crucially – costs of the new regime must all be weighed up, says Paul Harris at Pillsbury Law.
 
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Science & Innovation
Business Models

Eco Friendly

A new ecosystem model is rapidly evolving in pharma and life sciences. Heather Fraser at IBM explains how it will require a level of collaboration the industry has not engaged in before, transcending boundaries and stimulating a growth in innovation.
 
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DATA MANAGEMENT
Q&A: Investigator Site Data

Joint Ventures


Through collaborative efforts such as the Shared Investigator Platform, biopharma partners are working to lessen administrative burdens for investigators and enhance the patient experience. Jackie Kent of Eli Lilly and TransCelerate talks to EPC.
 
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Risk Management
Pharmacovigilance

Progress Report


EPC offers a run-down of specific measures being implemented by the EMA to maximise the efficiency of the EudraVigilance safety reporting system for adverse events, following a significant decline in signals in 2014.
 
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Research and Development
Preclinical Development

Non-Clinics: Progression

Exploring the changing face of non-clinical development, Envigo's Lee Coney looks at the intricacies of investigating the safety and pharmacology of biologic drugs before they enter clinical trials, and the essential role of CRO players.
 
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Published quarterly in
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News and Press Releases

PredictImmune announce issuance of new patent in the US in support of commercialisation

PredictImmune, developers of pioneering prognostic tools for guiding treatment options and improving patient outcomes in immune-mediated diseases, today confirmed its latest patent grant in the US. The US patent is part of PredictImmune’s third family of intellectual property (IP) relating to methods for predicting autoimmune disease risk. This follows successful grants across the company’s first family of IP in the UK and Europe in October 2018 and Canada in January this year.
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White Papers

Clinical Trials in Ukraine: Orange Paper Overview and 1st Half Year 2014

Synergy Research Group

The Orange Paper is an analytical report about the clinical trials market in Russia, published quarterly by the contract research organization Synergy Research Group. The first edition of Orange Paper was released in 2006, and at the moment 31 issues have already published. Now, thanks to Synergy Group Ukraine, obtaining information about the market of clinical trials in Ukraine has become possible. In Ukraine, during the period from 1996 to 2013, applicants had obtained 3,864 positive conclusions about the possibility of conducting clinical trials of drugs, both for domestic and foreign manufacturers, including conduct of multinational multi-center clinical trials (hereinafter – MMCTs)
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Industry Events

INTERPHEX 2019

2-4 April 2019, Javits Center, New York

At INTERPHEX, find all of the State-of-the-Art Solutions you need to Cost Effectively Develop and Manufacture Product. INTERPHEX is a premier pharmaceutical, biotechnology, and medical device development and manufacturing event and sponsored by Parenteral Drug Association (PDA). Dedicated to Innovation, Technologies and Knowledge, the show focuses on the entire product development life cycle.
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