About Clinical Trial Pharmacy
At the Clinical Trial Pharmacy (in Dutch: subdepartment Klinisch Geneesmiddelenonderzoek, KGO), we offer comprehensive support for all clinical trials involving with medicinal products, backed by extensive expertise in current legislation (GCP, GDP, and GMP). This includes both investigator-initiated studies and those sponsored by the pharmaceutical industry.
Services of KGO
- Advice
- Facilitating clinical trials involving medicinal products
- Preparation of manufacturing of medicinal products
- Storage and distribution of medicinal products
- Support during and after the study
Contact and timelines
To ensure optimal support, please submit your study request early using the application form. KGO will assess whether there is sufficient capacity to support your study and provide an indicative timeline.
Next, KGO will evaluate study feasibility and sign the Site Suitability Declaration (in Dutch: Verklaring Geschiktheid Onderzoeksinstelling, VGO). Following that, a pharmacy budget will be prepared. Once these steps are completed, the preparations for the start-up of the study will begin.
For investigator-initiated studies with Amsterdam UMC as the sponsor, a (hospital) pharmacist or trial coordinator will contact you to schedule an intake appointment to discuss feasibility of the study and the pharmacy budget.
Please note: the study will only be processed if the official application form is submitted.
Contact details:
- Submit your study: Amsterdam UMC Locatie AMC - Aanmelden studie kenniscentrum
- Questions about study start-up: opstart.kgo@amsterdamumc.nl
- Questions about ongoing studies at the AMC location: trial.apotheek@amsterdamumc.nl
- Questions about ongoing studies at the VUmc location: onderzoeksmedicatie@amsterdamumc.nl