- About us
- Regulatory Affairs
- Pharmacovigilance & Med. Affairs
- Quality & Manufacturing (GMP)
- Business Development
Case reports on adverse reactions associated with medicinal products need to be collected in a central validated database which allows for electronic reporting to authorities in accordance with the E2B standard.
We perform case collection, processing and reporting on your behalf using our own pharmacovigilance database.
For companies planing to operate their own database, we provide advise on which commercial database provider to chose.
Combining our long-time experience in regulatory affairs, pharmacovigilance, quality assurance and manufacturing with our excellent in-house understanding of computerised systems and software development, we provide comprehensive guidance during your IT projects.
We make sure that management, end users and software developers speak the same language and follow a common strategy.
Ensuring a professional project management, we help you
Our services also include: