Cand.med.vet/DVM, Senior Pharmacovigilance Manager
Rikke Heidmann holds a master’s degree in veterinary medicine from University of Copenhagen and is pursuing a post graduate diploma (PgD PV) within pharmacovigilance at University of Hertfordshire. Rikke has been with Billev Pharma since January 2025 as Senior Pharmacovigilance Manager.
Rikke has 12 years of experience as a veterinary clinician, primarily in companion animal acute medicine and surgery. Additionally, Rikke has years of experience teaching veterinary students and aspiring zoo-keepers.
Rikke has more than 11 years of experience with pharmacovigilance, primarily within human clinical trial patient safety at headquarter level.
- Setling safety data flow and processing for clinical trials
- Safety reporting and ICSRs handling, including medical assessment and company comment authoring
- Health Hazard Evaluations for non-conformities
- Training of colleagues, clinical trial HCPs and investigators
- Regulatory surveillance
Services
Registration
We are well-equipped to provide regulatory advice, discuss strategy and/or compile the registration dossier.
Pharmacovigilance
We have a team of highly qualified pharmacovigilance employees with expertise in all aspects of pharmacovigilance.
Translations
We offer high quality medical & pharmaceutical translations into and from several European languages.
Electronic submission
We are equipped to assist with any type of electronic submission and maintenance of your electronic file.
Special medicines areas
Herbal medicinal products, strong vitamin and mineral products, medicinal gasses, euphoriant substances, etc.
GDP & GMP Services
We offer full time and part time responsible person (RP) function and qualified person (QP) function.
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