Daniela Furnadzhieva

Marketing department at Huvepharma EOOD
  • Claim this Profile
Contact Information
Location
Lozenets, Sofia City, Bulgaria, BG

Topline Score

Topline score feature will be out soon.

Bio

Generated by
Topline AI

You need to have a working account to view this content.
You need to have a working account to view this content.

Experience

    • Marketing department
      • Mar 2010 - Present

      Promote veterinary products and distribute veterinary brochures and materials to different places and Huvepharma local offices in the world. Update the text of existing brochures and create the text of new ones through scientific research and reading of specific scientific articles. Promote veterinary products and distribute veterinary brochures and materials to different places and Huvepharma local offices in the world. Update the text of existing brochures and create the text of new ones through scientific research and reading of specific scientific articles.

    • Italy
    • Research Services
    • CRA grade I
      • Jan 2008 - Jan 2010

      To act as the primary support within the clinical project team thus ensuring the clinical trial is conducted in accordance with international regulatory and ethical guidelines for Good Clinical Practice. To assist the Project Manager and Senior Clinical Research Associate (SCRA) with the day-to-day conduct of running international clinical studies. To act as the primary support within the clinical project team thus ensuring the clinical trial is conducted in accordance with international regulatory and ethical guidelines for Good Clinical Practice. To assist the Project Manager and Senior Clinical Research Associate (SCRA) with the day-to-day conduct of running international clinical studies.

    • Drug Safety Officer
      • Jan 2007 - Sep 2007

      Working with SOP’s and ICH GCP guidelines Writing the SOP‘s and Flow charts for the Pharmacovigilance Unit Dealing with Serious Adverse Events information, contacting EMEA Research reading and process of the SAE information from sceintific articles connect with different investigational drugs and their date entry of the system Working with SOP’s and ICH GCP guidelines Writing the SOP‘s and Flow charts for the Pharmacovigilance Unit Dealing with Serious Adverse Events information, contacting EMEA Research reading and process of the SAE information from sceintific articles connect with different investigational drugs and their date entry of the system

Education

  • University of Hohenheim
    Master, Enviromental Protection and Agricultural Food Production
    2003 - 2006
  • Trakiyski universitet
    Master, veterinary medicine
    1993 - 1999

Community

You need to have a working account to view this content. Click here to join now