Events

15.09.2014 - 19.09.2014

14th International Conference on Plasma Surface Engineering

Garmisch-Partenkirchen (GER)

The biennial PSE conference series is organized by the European Joint Committee on Plasma and Ion Surface Engineering. PSE provides an opportunity to present recent progress in research and development and industrial applications. Its topics span a wide range from fundamentals such as e.g. process modelling and simulation of plasmas or thin film physics, through empirical studies which e.g. establish the relationships between process parameters and the structural and functional properties of modified surfaces and/or thin films, towards the application in industrial production.
Contact: EFDS e.V.
pse2014@efds.org

Quality by Design – New Concepts for Chemical and Biotech Product Development and optimisation

Media-Partner

22.09.2014 - 24.09.2014

Quality by Design – New Concepts for Chemical and Biotech Product Development and optimisation

Vienna (A)

As clinical trials become more complex and there is increasing demand for efficiency and cost effectiveness, the knowledge and skills required to manage all aspects of a clinical project are critical. This course provides a comprehensive foundation in clinical project management. Using the Project Management Body of Knowledge (PMBOK®) as a guide, participants will be taught how to apply project management strategies, tools and techniques to their clinical trial projects.
In two independent modules of three days each, the following topics will be covered:
- Project Definition and Organisational Context
- Project Management Tools and Techniques
- Scope Management, Resource Estimating and Budget Management of a Clinical Trial
- Project Quality Management
- Project Risk Management
- Communication and Stakeholder Management
- Procurement Management
- Team Management and Leadership Skills
This training course is geared toward professionals who desire a comprehensive foundation in clinical project management. Participants should have at least two years of clinical trial experience, or have completed the DIA training course “Essentials of Clinical Study Management.”
This "Clinical Project Management" training course is targeted at an intermediate/advanced level.
Contact: DIA Europe
Phone: +41 61 225 51 51, Fax: +41 61 225 51 52
diaeurope@diaeurope.org

Media-Partner

22.09.2014 - 24.09.2014

Training Course: Clinical Project Management - Part I

Paris

As clinical trials become more complex and there is increasing demand for efficiency and cost effectiveness, the knowledge and skills required to manage all aspects of a clinical project are critical. This course provides a comprehensive foundation in clinical project management. Using the Project Management Body of Knowledge (PMBOK®) as a guide, participants will be taught how to apply project management strategies, tools and techniques to their clinical trial projects.
In two independent modules of three days each, the following topics will be covered:
- Project Definition and Organisational Context
- Project Management Tools and Techniques
- Scope Management, Resource Estimating and Budget Management of a Clinical Trial
- Project Quality Management
- Project Risk Management
- Communication and Stakeholder Management
- Procurement Management
- Team Management and Leadership Skills
This training course is geared toward professionals who desire a comprehensive foundation in clinical project management. Participants should have at least two years of clinical trial experience, or have completed the DIA training course “Essentials of Clinical Study Management.”
This "Clinical Project Management" training course is targeted at an intermediate/advanced level.
Contact: DIA Europe
Phone: +41 61 225 51 51, Fax: +41 61 225 51 52
diaeurope@diaeurope.org

Translating the New Clinical Trials Regulation into Practice/Translating the New Transparency Requirements into Practice

Media-Partner

23.09.2014 - 25.09.2014

Translating the New Clinical Trials Regulation into Practice/Translating the New Transparency Requirements into Practice

London (UK)

Clinical Trials Workshop I and II – Combining Pricing
Workshop I will provide a forum for information exchange and discussion on conceptual and practical questions through lectures, panel discussions, and interactive break-out sessions. Day 1 will focus on the new provisions for submission, assessment and decision-making of clinical trial applications, and the management and monitoring of trials. Day 2 will focus on the new transparency provisions for clinical trials.
Workshop II on clinical data transparency will focus on practical considerations for the disclosure of clinical trials data. Attendees can participate in either one workshop or in the entire 3-day program. The two workshops will overlap with a day addressing the Transparency aspects of the Clinical Trials Regulation.
Contact: DIA Europe
Phone: +41 61 225 51 51, Fax: +41 61 225 51 52
diaeurope@diaeurope.org

Medical Approach in Diagnosis and Management of ADRs

Media-Partner

23.09.2014 - 24.09.2014

Medical Approach in Diagnosis and Management of ADRs

Paris

The 20th edition of this annual training course, considered by many experts as one of the pillars of medical training in pharmacovigilance, focuses on how to use medical knowledge in the diagnosis and management of selected Adverse Drug Reactions (ADRs). ADRs of the main systems/organs will be presented and explained by experts in their medical domain in order to provide practical clues to understand and manage the serious reactions in clinical trials a well as in post authorisation.
The medical approach presented in this training course will take into consideration the conclusions of international or national consensus meetings on adverse drug reactions.
Contact: DIA Europe
Phone: +41 61 225 51 51, Fax: +41 61 225 51 52
diaeurope@diaeurope.org

Diagnosis and Management of Drug-Induced Liver Injury (DILI)

Media-Partner

23.09.2014 - 24.09.2014

Diagnosis and Management of Drug-Induced Liver Injury (DILI)

Paris (F)

This new DIA training course is entirely dedicated to Drug-Induced Liver Injury (DILI). It is led by a Hepatologist with extensive experience in clinical assessment of DILI and who published ‘RUCAM’, the widely used causality assessment method of DILI. The course will cover the progress that has been made in the clinical detection and prevention of DILI in clinical trials and in post marketing phase. Regulatory guidelines need to be understood for an optimal assessment of DILI cases. Better use of typical tools will be emphasised in order to improve patient safety and drug monitoring in new drug development, especially in large populations. This course will provide tools, explanations, examples and several exercises for a better understanding of DILI and how best to apply that knowledge in day to day work.
Contact: DIA Europe
Phone: +41 61 225 51 51, Fax: +41 61 225 51 52
diaeurope@diaeurope.org

23.09.2014 - 24.09.2014

7th EPLS-Meeting

Prague (CZ)

The programme will include presentations from those within the industry together with the introduction of interactive sessions such as ‘talking tables’ and a panel discussion on Tuesday afternoon. There will be the traditional extended breaks to allow for informal networking throughout the event alongside the more formal one-to-one meeting area.
Contact: Pharmaceutical Licensing Group Ltd.

BioSpain 2014

Media-Partner

24.09.2014 - 26.09.2014

BioSpain 2014

Santiago de Compostela (ES)

International Meeting on Biotechnology – trade exhibition, partnering event, investment forum, scientific congress, top level seminars & conferences and a career fair with a well balanced mixture of local and international private companies, universities, overseas clusters, research institutes and governmental bodies.
Contact: David Fernandez, asebio
dfernandez@biospain2014.org

EFIB 2014 - The European Forum for Industrial Biotechnology and the Biobased Economy

Media-Partner

30.09.2014 - 02.10.2014

EFIB 2014 - The European Forum for Industrial Biotechnology and the Biobased Economy

Reims (F)

Organised by EuropaBio and Smithers Rapra, in association with IAR, the annual EFIB congress will attract 800 stakeholders of the biobased economy to come together to explore the potential of industrial biotechnology, network with leaders and influencers in this sector and hear from key policymakers shaping the future of the European bioeconomy.
 
See www.efibforum.com for more information on what this leading event has to offer in the heart of the Champagne-Ardenne region.
Contact: Hayley Marsden, Smithers
Phone: +44-1372-802000
hmarsden@smithers.com

05.10.2014 - 08.10.2014

HUPO 2014

Madrid (E)

13th Human Proteome World Congress – The challenge of defining and understanding proteomes in the context of cell biology is huge and requires a multidisciplinary effort to ensure innovative technical developments, the generation of biological information as well as the integration and interpretation tools to transform the information into biological knowledge. The Congress is an ideal environment where international experts can discuss all these aspects generating new ideas and establishing productive scientific interactions.
Contact: Human Proteome Organization

06.10.2014 - 08.10.2014

Max Rubner Conference 2014 – Enzymes in Food Processing

Karlsruhe

The conference aims to provide an updated overview on the applications of enzymes in the food sector, and of progresses made in respect to exploit more efficient biocatalysts, through screening, structural modification, and immobilization of enzymes. Targeted improvements aim at enzymes with enhanced thermal and operational stability, improved specific activity, modification of pH-activity profiles, and increased product specificity, among others. Besides technological aspects, legal and health issues are also addressed.
Contact: Max Rubner-Institut – Bundesforschungsinst. f. Ernährung u. Lebensmittel
Phone: +49-721-6625-611
mrc@mri.bund.de

European Biotech Week 2014

Media-Partner

06.10.2014 - 12.10.2014

European Biotech Week 2014

B/FIN/F/IRL/IT/LIT/NL/CH

The story of European Biotechnology – Biotech National Associations, in collaboration with companies, academic and government institutions, science museums and the media, organised biotech events right across Europe.
Contact: Rosalind Travers, EuropaBio
r.travers@europabio.org

© 2007-2014 BIOCOM

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No liability assumed, Date: 18.09.2014


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