How can we Help?

  • 01

    Local contact person for PV, including deputy and/or back-up PV person

  • 02

    Quality Control of translations and transcription for safety-related information

  • 03

    AE Processing - Case intake and follow-up

  • 04

    PV Training

  • 05

    PV Intelligence

  • 06

    Product Safety Information from Literature

  • 07

    Monthly Reconciliation

  • 08

    PSMF Updates

  • 09

    RMP and RMM

  • 10

    Vendor management

  • 11

    Report into EudraVigilance Database

  • 12

    Submit and retrieve medicinal product data using the extended EudraVigilance medicinal product dictionary (XEVMPD), the Article 57 database. This is aimed at ensuring the quality of data in the XEVMPD on authorized or investigational medicinal products.

We’d love to hear more about your needs

Even if you are still in the planning stages of your project, you are more than welcome to submit a request to us. We can assist you with a quotation or create a proposal for you based on the minimum of information you can provide.

RFP - RFI

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CEBIS Interantional

Romania- Helios Business Center (HBC),
47 Bd. Theodor Pallady,
Bucharest, Romania