Clinical Trials

Pharmaceuticals

HPZenner Clinical Trial Unit

Hands-on experience conducting clinical trials for pharmaceuticals since 1986.

• Submissions to BfArM/ethics committees, conduct, monitoring, statistical and clinical analysis and ICH-compliant reporting — through to publication in scientific journals
• Trial unit in Germany for organising inpatient and outpatient clinical trials
• Legally independent German Study Unit of Prof. Dr. med. Zenner for outpatient conduct of clinical trials
• Certified coordinating investigators, principal investigators and trial physicians with a trial site in Tübingen
• International network of coordinating investigators in Germany, the EU, Japan, South Korea and the USA for multicentre trials

Medical Devices

CRO for the entire study development

• Study development per ISO 14155/MPKPV/DiGAV, submissions per MDR/MPDG/DiGAV incl. BfArM/ethics committees
• Conduct, monitoring, statistical and clinical analysis and ICH-compliant reporting of clinical trials of medical devices — through to publication
• Broad spectrum of evaluated and tested medical devices — see the overview here
• DiGA expertise: clinical trials and evaluations of DiGAs are among HPZenner’s specialties — learn more