
M.Sc. Pharmaceutical Sciences, Senior Pharmacovigilance Manager &
QPPV – Human accounts
Laura Sparving holds a B.Sc. in Pharmaceutical chemistry and a M.Sc. in Pharmaceutical Sciences. Laura has been with Billev Pharma since December 2025 as Senior Pharmacovigilance Manager and QPPV – Human accounts and previously 5 years with Billev Pharma as Pharmacovigilance Manager/QPPV and deputy QPPV – Human accounts/Deputy QPPV – Veterinary accounts.
Laura has 16 years of experience within Pharmacovigilance, both post-marketing and clinical trials for human medicines within the following areas:
- QPPV and deputy QPPV roles
- Safety committee chair and product safety lead
- Safety representative in clinical development programmes
- Safety representative in submission teams
- Signal detection
- Aggregated report authoring (PSURs, DSURs, RMPs)
- Case processing
- Literature surveillance
- Training of internal and external colleagues
- Co-auditor
Furthermore, Laura has experience with Veterinary Pharmacovigilance as Deputy QPPV and 2 years of experience within Regulatory Affairs.
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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