GxP Services
The University of Zurich provides the full pipeline of drug and medical device development services from Good Laboratory Practice (GLP), Good Manufacturing Practice (GMP) to Good Clinical Practice (GCP) .
Grid containing content elements
GLP ensures the quality, consistency, and integrity of non-clinical laboratory studies used for safety and regulatory submissions.
GMP governs the controlled production of medicines and therapeutic products to ensure their safety, quality, and compliance with regulatory standards.
GCP provides an ethical and scientific framework for designing, conducting, and reporting clinical trials involving human participants, ensuring their rights and data integrity are protected.