Elvira Graat Email & Phone Number

Boxmeer, Noord-Brabant, Nederland

• preparing and submitting registration procedures of veterinary medicines (new applications, renewals, variations)• coordinating and implementing of revised and new product labeling• translating of product information (SPC, PIL, label) • reviewing and approving promotional material• communicating with relevant stakeholders, e.g. packaging sites, marketing• setting up and maintaining contacts with competent authorities

Nijmegen, Gelderland, Nederland

Eindhoven Area, Netherlands

Responsible for pharmacovigilance and regulatory affairs activities for several pharmaceutical companies

Responsible for triaging and processing of adverse event information according to Standard Operating Procedures (SOPs) for reporting to the regulatory agencies.

Responsible for trial administration, verification, validation, Serious Adverse Event (SAE) handling and quality control of the SAS programming and output.

Responsible for data analysis for the health insurance industry by using SAS programming