Clinical Investigation Unit

The UIC has been ISO 9001-certified since 2012.

Over 120 clinical studies supported 


120 m2 dedicated to conducting clinical studies; up to 9 care beds available

  • Investigator support:
  • Pharmacokinetic studies
  • Neurophysiological exams
  • Physiopathological studies
  • Drafting study documents, protocols, case report forms (CRFs), standard operating procedures (SOPs)
  • Designing and submitting documents to authorities
  • Recruiting patients
  • Project management
  • Data collection/entry
  • Storing and dispensing study products
  • Monitoring
  • Processing, storing and sending biological samples
  • Pharmacovigilance, Data Safety Monitoring Board (DSMB)
  • Data Management 


  • Dre Angela Huttner, MD, Head of the CRC Clinical Investigation Unit 
  • The team includes clinical research associates, research nurses, physicians, pharmacists and data managers 

Contact HUG / Rue Gabrielle Perret-Gentil 41211 Geneva 4 Tel. 022 372 91 34Fax: 022 372 91 35

How can I submit a request?

By email to


Beds Building, STERN, Unit 4 AL, 4th floor 


Bâtiment des lits, Unité 4 AL

The Clinical Investigation Unit collaborates with the Clinical Pharmacology and Toxicology Division.