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IMPORTANT DATES

Please refer  to EBMT Related Meetings for more information about a specific  meeting

  • 6th-9th July
    ESH-EBMT Euroconference.
    ¨GvHD/GvL: A paradigm of Haemopoietic Stem-Cell Transplantation¨ ES
  • 15th-19th September

    Leukaemia & Lymphoma.
    'East and West Together' HR

  • 23rd -27th September

    The 14th European Cancer Conference.
    “Cancer in Europe - sharing the responsibilities” ES

  • 24th-26th September
    International Symposium - Bioengineering and Regenerative Medicine, FR
  • 24th-28th September
    Advances in Haematology - 39th Annual Course, UK
  • 4th - 6th October

    5th Workshop on Haploidentical Stem Cell Transplantation, IT

  • 16th - 20th October
    Turkish Haematology Society – National Haematology Congress, TR
  • 17th-20th October

    AlloStem-ESH-IWP Training Course on Immunotherapy for Stem Cell Transplantation, ES

  • 19th – 21st October
    ESH-EUROCORD-NETCORD
    EBMT-UT MD Anderson Cancer Centre Conference. ¨Biology & Clinical Applications of Cord Blood Cells¨ ES
  • 25th -27th October
    10th Infectious Diseases Working Party Training Course

Association News

 

 

 

Who’s Who at…..The EBMT Clinical Trials & Study Office,Leiden,The Netherlands

 

 

Two major streams (Prospective Clinical Trials and Observational Studies of the CLWP) are working together in Leiden under the leadership of Anja van Biezen. The Prospective Clinical Trial Group tasks are: protocol & CRF development, regulatory issues, programming of databases and quality controls, randomization of patients and entry of trial data. Clinical Trial SOP development is a general task.

The Observational CLWP study group retrieves data from ProMISe2, prepares files for data requests, checks and enters the collected study data, prepares final data files for analyses and creates plots for manuscripts. Data quality control is a general task.

Main Address:

EBMT Clinical Trials & Study Office
Department of Medical Statistics & Bioinformatics
Postzone S-05-P
LUMC
PO Box 9600
2300 RC Leiden
The Netherlands

Phone +31 71 526 9724
Fax 1: +49 180 500 290 623 (fax to e-mail system)
Fax 2: +49 711 4900 8723 (fax to e-mail system)

Name: Anja van Biezen

Title: Clinical Trials & Study Office. Co-ordinator

Responsibilities: Statistical analyses, Observational Study Co-ordination, Office Management.

Contact for: CLWP registry     
Email:  clwpebmt@lumc.nl

 

 

Name: Miriam van Gestel

Title: Study Co-ordinator

Responsibilities: Data Management CLWP

Contact for: CLWP Observational Studies
Email:  clwpebmt@lumc.nl

 

 

Name: Anja Henseler

Title: Study Co-ordinator

Responsibilities: Data Management CLWP

Contact for:  CLWP Observational Studies
Email: clwpebmt@lumc.nl

 

 

Name: Menno van den Bosch

Title: Data Manager

Responsibilities: Data Entry

Contact for: Data Entry Issues
Email:   clwpebmt@lumc.nl

 

 

Name: Marleen van Os

Title: Senior Clinical Trials Co-ordinator

Responsibilities: Prospective Trial Co-ordination and Data Management

Contact for: Prospective Clinical Trials
Email:  clwpebmt@lumc.nl

 

 

Name: Alain Barrois

Title: Clinical Trials Co-ordinator

Responsibilities: Prospective Trial Co-ordination and Data Management

Contact for: Prospective Clinical Trials
Email:  clwpebmt@lumc.nl

 

 

Name: Thekla Jansen

Title: Database Co-ordinator
Responsibilities: Prospective and Observational. Database management

Contact for: Data base Management Prospective Clinical Trials/Observational Audits
Email: clwpebmt@lumc.nl

 

 

Name: Ronald Brand

Title: Statistician

Responsibilities: EBMT Statistician

Contact for: Statistical Analyses
Email:  r.brand@lumc.nl

 

 

Name:: Simona Iacobelli (stationed in Rome)

Title: Statistician

Responsibilities: Statistical Analyses of the Multiple Myeloma Sub-Committee CLWP

Contact for: Statistical Analyses MM
Email:  clwpebmt@lumc.nl

 

 

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