Bioforum provides medical writing services to projects of early and late phase product development. These include study-specific documents and development-program documents. The medical writing service is fully integrated into multi-disciplinary clinical development teams, specifically safety, biostatistics and data management aimed at producing the highest-quality, most regulation-compliant, clear and informative documents while adhering to timelines.
Bioforum’s Clinical Data Management team is fully committed to providing high-quality and reliable services using the industry’s leading technology designed for quality data capture.
We manage all aspects of your data – from study startup to submission, and closely collaborate with clinical teams ensuring they meet the timelines and milestones of their trial.
Our clinical programmers have vast experience with many therapeutic areas and indication across different study phases and constantly keep up with current guidance and developments as they pertain to data standards and regulatory demands.
The complementary biostatistical services, including SAP Development, SAS Clinical Programming, Analysis, Submission-Ready Services and Statistical Reports are customized and designed specifically to meet the project requirements
We provides all the pharmacovigilance services required for your clinical trial. Pharmacovigilance – also known as drug safety – describes the collection, analysis, monitoring and prevention of adverse effects in drugs and therapies, and is an essential function within a life science company.