Consulting: Personal consulting regarding Good Clinical Practice (GCP), Good Manufacturing Practice (GMP), Pharmacovigilance, ISO 9001 and regulatory compliance of clinical trials.
Audits: Verification of study specific procedures and respective documentation regarding completeness and traceability in the framework of general CCP audits or in preparation of inspections by regulatory authorities. More...
Documents: In the framework of Guidelines of Clinical Research templates and guidelines for all aspects of clinical research are made available to researchers of the UniversityHospital Zurich.
QMS Transfer: Within the General Strategy Highly Specialized Medicine of the Canton of Zurich we support University of Zurich-associated hospitals and collaboration partners in the Canton of Zurich in establishing and improvement of local operative Quality Management Systems for clinical research.