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| home > ebr > Autumn 2004 |
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 PUBLICATIONS |
European Biopharmaceutical Review |
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| At the cutting edge of the latest industry developments, Samedan is adept at keeping the information you need at your fingertips. EBR provides a unique platform of communication for the market across Europe, North America and the rest of the developed world. To find out what's hot in the world of of biopharmaceuticals, take a look below at the range of articles featured in this issue of EBR. |
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| In her Editor's Letter, Dr Helen Tayton-Martin takes a look at the topics in this issue |
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| Dr Majid Mehtali, Vice President of Research & Development at Vivalis SA, underlines the potential of Embryonic Stem Cells: Current and Future Industrial Applications |
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| Unravelling the Mysteries of Alzheimer's - the search for a cure continues, by G Steven Burrill, CEO of Burrill & Company |
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| Sunil Saini, Director of Biomaterials at Therics, maps the development of a new domain in A Perspective in Orthopaedic Tissue Engineering |
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| Hans Herklots, Media and Investor Relations Director at IsoTis OrthoBiologics, looks at the potential transformation of orthopaedics, in Biologics are Entering the Orthopaedic Arena |
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| How are ideas transformed into a thriving business? Nigel Wild, Managing Director of Oxfordshire BioTechNet Ltd, discusses the options in Funding and Mentoring - The Keys to the Biotech Kingdom |
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| In Technology Transfer from Universities, Tom Hockaday, Executive Director of Isis Innovations Ltd, welcomes the continuing interest in collaboration between academia and the business community |
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| Incubators must form an integral part of our infrastructure for supporting young companies, asserts Toni Wanklin, Development Manager at UK Business Incubation, in Breaking Through The Barrier: How Bio-Incubators Support Tomorrow's World-Class Entrepreneurs |
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| Fiona Brown, Public Relations Consultant, considers today's funding environment and the particular hurdles inherent in biotechnology in Uniting Science and Business: The Challenges for Biotech Start-ups |
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| Science, finance and IPR: conditions for Finnish entrepreneurs uncovered in Challenges for Biotech Start-Ups: A Nordic Perspective, by Professor Kalevi Kairemo, Medical Director and Dr Oula Pe-ate Medina, CEO of CTT Cancer Targeting Technologies |
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| Continuing from Part 1 in our summer issue, Beyond Financial Analysis - Scientific Due Diligence in Pharma and Biotech: Part 2 focuseson clinical trials. By Dr Konrad Burk, Founder of ClinDescience GmbH, William McCulloch, CMO of Gloucester Pharmaceuticals, Dr Alexander von Nieciecki, CEO of BioProof, and Dr Wolfgang Meyer, Senior Director of European Drug Regulatory Affairs and Dr Benno Rattel, Senior Director of Drug Development at GPC Biotech AG |
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| Valuing Innovation: Patient Access to Novel Therapies, by Alastair Kent, Director of the Genetic Interest Group, explores the disjunction between scientific advances and practical resources |
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| Dr Sarah Rawlings, Policy and Information Officer at Breakthrough Breast Cancer, examines the 'postcode lottery' of UK health care in NICE Implementation - The Patient Perspective |
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| Dr Stephen Hammond, CEO of Scottish Biomedical, investigates the factors to be weighed in the Successful Outsourcing of Preclinical Drug Discovery |
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| In Electronic Diary Solutions: Enhanced Collection of Patient Reported Outcomes Data, Dr Bill Byrom, Product Development Director at ClinPhone Group Ltd, details alternatives to the traditional paper-based diary that can reduce the likelihood of distorted results |
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| Ivan N Rich, Founder, Chairman and CEO of HemoGenix, Inc, discusses Stem Cell Haemotoxicity Testing to Predict Toxic Side-Effects and as a Tool for Safety Monitoring during Drug Development |
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| Dr Wendy M Shaw, Associate Director (Europe) of the Late Phase Group at Kendle International Inc, explains the function of post-marketing surveillance in recording and studying new adverse drug reactions in Opportunities and Challenges of Pan European Post-Marketing Surveillance Programmes |
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| Identifying Appropriate RNA Interference Drug Candidates opens the door to a whole new class of treatments - by Dr David A Bumcrot, Director, Preclinical at Alnylam Pharmaceuticals, Inc |
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| Angelika Bonin-Debs, Director of Business Development and Strategic Alliances at Xantos Bioscience, charts the advent of RNAi and its role in Loss-of-Function and Gain-of-Function - Two Complementing Genome-Wide Technologies For Drug Discovery and Target Validation |
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| Automation and Robotics in High Throughput Protein Crystallography explained by Bernhard Rupp, Macromolecular Crystallography and Structural Genomics Group of the Lawrence Livermore National Laboratory, University of California |
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| Methods of column protection are presented in Syringe Filter Efficiency and the Effect of Filtration on HPLC Column Life, by Dr Weibing Ding, Senior Staff Scientist and Larry Scheer, Business Development Manager at Pall Corporation |
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| Regu Chandar Gnanapragasam, Assistant Manager of the Industrial & Trade Division of the Penang Development Corporation, Simon Saxby, Chief Executive Officer at Alpha Biologics Sdn Bhd and Dr Malcolm Blackwell, Chief Executive Officer at Progenix Research Sdn Bhd, unveil a new development zone for biotech in Malaysian Biotechnology Initiative for the State of Penang |
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| Innovation, investment and government support - Nicola Watkinson, Senior Investment Commissioner, Europe, at Invest Australia, sets the scene in Australian Biotechnology - An Untapped Opportunity |
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| CMP Information anticipate this year's BioTech Hot Spot, a unique networking facility at CPhI Worldwide/ICSE |
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| Answering the growing need for partnership opportunities, BIO-Europe 2004: Europe's Largest Partnering Conference, Provides a Platform for Deal-Making and Investors |
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| Tracing global industry trends in Resurgent, Refocused and On the Threshold - Insights from Ernst & Young's 11th Annual Global Biotechnology Report, by EBR Editor Helen Tayton-Martin |
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| Advokat Lars Rambe, Head of Life Science at Adokatfirman Delphi & Co, compares IP systems in the EU and US in Commercialisation of Inventions from Scandinavian Universities - A Challenge and an Opportunity |
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News and Press Releases |
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BioIVT Introduces New Quality Management System to Maintain Highest Quality Biospecimens and Drug Development Research Services
BioIVT, a leading provider of research models and services for drug and diagnostic development, today announced that it is introducing a new internal cloud-based Quality Management System (QMS), Master Control. This new standardized, ISO compliant QMS will help BioIVT manage documentation, auditing, supplier and customer accounts, and risk across all locations. It will consolidate and replace a variety of computer- and paper-based document control systems located at existing and newly-acquired BioIVT sites in the US, Europe and Asia.
More info >> |
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White Papers |
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Systems Engineering for Complex Portable Medical Device Development
Phillips-Medisize
As the demand for complex, portable medical devices continues to grow, reducing risk and increasing efficiency during the development of these products should be paramount. Taking a systems-engineering (SE) approach to development provides a holistic, organized, and deliberate method for identifying as well as reducing both patient and business risks early in the process. Furthermore, it facilitates efficient progression throughout the entire product development life cycle.
More info >> |
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Industry Events |
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Outsourcing Clinical Trials Nordics 2018
30-31 October 2018, Copenhagen, Denmark
Following on from the success of the 2017 Outsourcing in
Clinical Trials Nordics conference, Arena International is pleased to announce
that the event will return for its 6th year in 2018.
The 2018 event welcomes biopharmaceutical and medical device
companies from across the Nordic region to share knowledge and challenges of
outsourcing and clinical operations.
More info >> |
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