22 - 23 May 2013
With more and more clinical trials carried out in the Russia, CIS, MENA and Turkey regions, it is essential to know - What are the pitfalls and how can they be overcome? What mistakes have others made and what can be learned? This event has been designed to answer the above questions – with practical strategies to take back to the office and implement, and two agendas packed full of real-life experience, from both locally based country-experts and Western European based clinical professionals.
"Having been involved with the Infotech conference in the past, I am very excited to see its return. It was THE meeting in Europe for informatics and IT professionals working in pharma and biotech R&D. I very much look forward to the conference being re-established during this transformational period, when we struggle with unprecedented data volume and complexity in supporting scientific and clinical decision making."
"Excellent talks and very important topics"
Healthcare Insurance & Group Risk Protection
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Medical Device and IVD Regulations in Asia Pacific
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Discover the latest in screening technologies, developability, linker technology, novel payloads and process development considerations to ensure product market approval
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Empowered Antibodies
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RABs and Bispecific Antibodies
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Company Core Data Sheets
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Raw Materials
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Safeguard your production facilities and raw materials against adventitious agents by optimising your viral detection, inactivation and removal methods in line with regulations
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Genotoxic Impurities
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INFOTECH
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How to initiate, plan and implement successful projects
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Global Chemical Regulations
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Agrochemical Formulation USA
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Plant Biotechnology USA
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Biopesticides
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European Chemicals Policy & Risk Management
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Biocidal Products Regulation
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Regulation of Veterinary Medicines and Generics in Europe
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CIR
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Bioanalytical Congress
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Analytical Method Development, Validation and Transfer
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Modified Release in Oral Drug Delivery
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Pre-Filled Syringes & Novel Injector Devices
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Formulation Strategies for Pharmaceuticals
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Inhalation Drug Development
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Post-Approval Studies
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Pharmaceutical Labelling
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Labelling Compliance for Medical Devices and IVDs
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Bio-Production
More InfoBiosimilars in Turkey, MENA, Southeast Asia, India & Russia
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Partnerships in Clinical Trials 2013
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