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BioForum offers a complete range of Clinical Data Management Consulting Services for Clinical Trials for Parmaceutical and Medical Device Development.
Our experts provide high-quality, comprehensive services that meet customer's specific requirements.

Services include:
 
  • Protocol writing
  • Case Report Form (CRF) design/consultancy
  • DOE (Design of Experiment): pre-clinical and clinical
  • Data Management Plan and CRF guidelines generation
  • Database design
  • Double Data entry
  • Electronic Data Capture projects
  • Edit checks/queries generation and resolution
  • Data Management Validation (DMV) and quality assurance
  • Coding of Medical Events
  • Data listing and reporting
  • Data Management Training and Consultancy
  • Regulatory strategy


 
Training Services:
A range of courses on various topics related to Data Management, both open-to-the-public and in-house, including:
 
Providing high standard services
Professional input Complying with:
  • Customer unique needs
  • Regulatory requirements

Head of Clinical Data Management - Tali Azulay:

Tali holds an M.A. in Experimental Psychology from Bar Ilan University, and B.A. in Psychology from Ludwig-Maximilians University, Munich, Germany.

Tali has an extensive experience in the data management of phase I to IV studies and the preparation of SOPs for the data management process.

Tali also serves as an adjunct lecturer at the department of criminology, Bar-Ilan University

For more information please contact Ms. Tali Azulay, talia@bioforum.org.il
Phone: +972-8-9313070, Mobile: +972-52-649-9017, Fax: +972-8-9313071

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