Events

31.10.2014 - 01.11.2014

IMED 2014

Vienna (A)

The International Meeting on Emerging Diseases (IMED 2014) is organized by the International Society for Infectious Diseases (ISID) and its Program for Monitoring Emerging Diseases (ProMED-mail). Emerging infectious diseases are at the center of the world’s attention. The threats posed by pandemic influenza, bioterrorism and the realization that new infectious diseases may be recognized at any time, in any place, have dramatically raised our awareness and our need to understand emerging pathogens. What are the most important emerging disease threats? What biological, ecological, social and other factors lead to their emergence? How can we quickly detect their occurrences in order to respond in timely and appropriate ways? This meeting will fully embody the “one health” model of emerging diseases, recognizing the commonality of human and animal health.
Contact: Doris Steinbach, International Society for Infectious Diseases
Phone: +43 1 481 19 48
doris.steinbach@isid.org

02.11.2014

China Forum 2014

Frankfurt am Main (GER)

A BIO-Europe pre-conference: What does it take to succeed in the 2nd largest healthcare market? The event brings together China-based life science executives with ther counterparts from Europe and across the globe.
Contact: Thomas Voigt, EBD Group
Phone: +1-760-930-0500
tvoigt@ebdgroup.com

Signal Management in Pharmacovigilance (Training Course)

Media-Partner

03.11.2014 - 04.11.2014

Signal Management in Pharmacovigilance (Training Course)

Paris (F)

Signal Management is a critical process of Pharmacovigilance required by EU Good Pharmacovigilance Practice. It is the scientific component that underpins Pharmacovigilance, and the very reason why Pharmacovigilance was created in the first place. The entire course has been updated in line with the latest guidelines on EU Good Pharmacovigilance Practices (GVP): Module IX - Signal management, Commission Implementing Regulation (EU) No. 520/2012, and CIOMS VIII. Time has been set aside for exercises, questions and discussions. The course will teach basic concepts of signal detection and signal management and how to apply them within the participants' functions. Data mining techniques for large volume ADR data analysis and relevant EMA guidelines will also be a discussed, as well as a future outlook.
Contact: DIA Europe
Phone: +41 61 225 51 51, Fax: +41 61 225 51 52
diaeurope@diaeurope.org

Essentials of European Regulatory Affairs (Training Course)

Media-Partner

03.11.2014 - 04.11.2014

Essentials of European Regulatory Affairs (Training Course)

Paris (F)

This is the must-attend training course for anyone needing to learn the essentials of European Regulatory Affairs - it has been extended to two days to include more topics, and it is kept up to date in minute detail by the experienced faculty.
The course will give an overview of the European regulatory system for human medicines, including the legislative processes and European Networks, the different routes for obtaining a licence for the European market, the centralised, the decentralised and the mutual recognition procedures, and the national procedures. In addition the specific European procedures for orphan drugs, paediatrics, advanced therapies and combination products will be discussed. This will cover the different steps and timelines in the different procedures, the clock-stops, the compiling of questions etc. An introduction regarding the lifecycle will be given by information in respect to pharmacovigilance, variations and renewals.
Contact: DIA Europe
Phone: +41 61 225 51 51, Fax: +41 61 225 51 52
diaeurope@diaeurope.org

How to Prepare for Pharmacovigilance Audits and Inspections (Training Course)

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03.11.2014 - 04.11.2014

How to Prepare for Pharmacovigilance Audits and Inspections (Training Course)

Paris (F)

Every pharmacovigilance function will, at one time or another, undergo governmental or health authority inspections as well as audits by license partners, internal auditors and others. The course will teach how to prepare for an audit / inspection from the time of the receipt of the announcement (or of the arrival of the inspectors at your doorstep) to the conclusion of the audit or inspection.
Contact: DIA Europe
Phone: +41 61 225 51 51, Fax: +41 61 225 51 52
diaeurope@diaeurope.org

BIO-Europe 2014

Media-Partner

03.11.2014 - 05.11.2014

BIO-Europe 2014

Frankfurt am Main (GER)

Biotechnology partnering conference. BIO-Europe features the industry’s most advanced Web-based partnering system, enabling delegates from all parts of the biotechnology value-chain to quickly identify, engage and enter into strategic relationships that drive their business successfully forward.
Contact: Thomas Voigt, EBD Group
Phone: +1-760-930-0500
tvoigt@ebdgroup.com

Essentials of Clinical Study Management (Training Course)

Media-Partner

05.11.2014 - 07.11.2014

Essentials of Clinical Study Management (Training Course)

London (UK)

The success of a clinical study is very much dependant on its efficient preparation and effective conduct. Study managers should be knowledgeable about required quality and regulatory standards, roles and responsibilities of team members, and be able to select and oversee internal and external resources. Study managers also should be able to anticipate potential problems, offer creative solutions and develop strategies to mitigate risk. This training course provides a comprehensive overview of the essential elements of study management and the clinical study environment in the context of the overall drug development process. After successful completion of the training course, participants will be able to plan, execute and manage a clinical study from protocol to final report.
Contact: DIA Europe
Phone: +41 61 225 51 51, Fax: +41 61 225 51 52
diaeurope@diaeurope.org

06.11.2014

EVCA Venture Capital Forum 2014

Berlin

Cross-sector venture capital event. As participants are expected early stage to late stage/growth capital VC firms investing across all industries to join to debate the unique challenges and opportunities of investing and operating in Europe.  
Contact: European Private Equity and Venture Capital Association
events@evca.eu

ISPE/DIA Workshop on Computer Systems Compliance – Maintain Data Integrity to Reduce Risk for the Patient

Media-Partner

06.11.2014 - 07.11.2014

ISPE/DIA Workshop on Computer Systems Compliance – Maintain Data Integrity to Reduce Risk for the Patient

Basel (CH)

This 2-day conference will provide a forum for information, discussion on conceptual and practical questions and experience exchange through lectures, panel discussions, and interactive workshop sessions. It will focus on the work being conducted by two leading organisations within the life sciences sector who approach the subject from differing directions but with the same clear objective of ensuring data integrity to reduce the risk to the patient. It will focus on the well-established approaches used, identifying the similarities of key principles and practice, and the challenges facing the industry with the availability of new technologies such as cloud computing.
Contact: DIA Europe
Phone: +41 61 225 51 51, Fax: +41 61 225 51 52
diaeurope@diaeurope.org

Benefit/Risk Management Training Course

Media-Partner

10.11.2014 - 11.11.2014

Benefit/Risk Management Training Course

Barcelona (ES)

The balance of benefits and risks of a product is the basis for all key decisions in the pharma industry. Thus the balance must not be left to chance – it can be and should be effectively managed. This intensive course explores current opportunities made possible by the new legislation, advances in information technology and a new scientific methodology to enhance and modernise the approaches in the product lifecycle management.
Contact: DIA Europe
Phone: +41 61 225 51 51, Fax: +41 61 225 51 52
diaeurope@diaeurope.org

Clinical Project Management - Part II

Media-Partner

10.11.2014 - 12.11.2014

Clinical Project Management - Part II

Barcelona (ES)

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

11.11.2014

Arctic Bioeconomy – Focus on West-Nordic Countries

Reykjavik (IS)

The conference is supported by The Nordic Council of Ministers Arctic Co-operation Programme, NKJ (Nordic Joint Committee for Agricultural and Food Research) , AG-Fisk (Working Group for Fisheries Co-operation), SNS (Nordic Forest Research) and NordGen (the Nordic Genetic Resource Center), as part of the project Arctic bioeconomy.The key note speaker Dr. Dr. Christian Patermann is an former director at DG Research European Commission, Biotechnology, Agriculture, Food Research and "Father " of the Bieoeconomy in Brussels. Further he is a former member of the 1st German Bioeconomy Advisory Council.
Contact: Matís ltd. - Icelandic Food and Biotech R&D
matis@matis.is

12.11.2014

Swiss Biotech Finance Day

Zürich (CH)

This event will give an overview over different issues with huge financial impact in company development. Financial frame and planning, development and regulatory costs, human resource issues are just some of the topics that finally influence your company’s budgets and not least valuation.
 
Contact: Swiss Biotech Association

EuroPLX 56 – European Pharma License Exchange

Media-Partner

17.11.2014 - 18.11.2014

EuroPLX 56 – European Pharma License Exchange

Nizza (F)

The partnering scope ranges from innovative to generic, from early stage candidates to approved, prescription or OTC drugs, medical devices and companion diagnostics. Delegates determine the focus, displayed and updated hourly on Internet as soon as sufficient data are submitted.
Contact: Dr. Norbert Rau, RauCon

PharmaLab 2014

Media-Partner

19.11.2014 - 20.11.2014

PharmaLab 2014

Düsseldorf (GER)

The PharmaLab Congress will cover various topics in 10 interesting conferences and lectures on analytics, bio analytics, microbiology and R&D. Parallel to the conferences, attendees will have the possibility to get to know companies exhibiting between the different conference rooms.
Contact: Wolfgang Heimes, Concept Heidelberg
Fax: +49-6221-84-44-21
info@concept-heidelberg.de

19.11.2014 - 20.11.2014

CLIB 2021 International Conference 2014

Düsseldorf

The conference will discuss aspects of the emerging value chains that are currently in focus of the European Horizon2020 program, for example in the public private partnerships BBI & SPIRE. These value chains are also addressed by the BIG-C initiative of Flanders, the Netherlands and North Rhine-Westphalia: From lignocellulosic feedstock to bio-based chemicals; CO2 and exhaust gases to chemicals; The next generation agro-based value chains; New value chains from organic side streams.
Contact: Cluster Industrielle Biotechnologie e.V.
Phone: +49 211 6793141
info@clib2021.de

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No liability assumed, Date: 30.10.2014


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