Data management

The effective and regulatory-compliant management of clinical trial data is an essential component of drug and device development.

Whether for regulatory submission, publications, or periodic safety update reports, your clinical trial data must have be high-quality and available in real-time.

BioForum CDmC's services cover all aspects of clinical data management, including (e)CRF design, entry screens design, data entry, data validation and coding of medical events.

We use the Good Clinical Data Management Practice (GCDMP) (www.scdm.org), the current industry standard for clinical data management, as a guide for our activities.

Our services comply with GCP and other regulatory standards.

Our data management services include: