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 information you can provide.