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Monitoring service for investigator-initiated clinical studies

Clinical Research Institute HUCH Ltd offers monitoring services for investigator-initiated clinical studies. 

Regular quality control is performed according to the regulatory requirements, the principles of good clinical practice (ICH-GCP) and the standard operating procedure of Clinical Research Institute HUCH Ltd. The investigator can determine the level of needed quality control in the study.

The investigator should contact the study monitor in early stage when planning a clinical study. The level and nature of monitoring are determined separately for each study in a study specific monitoring plan.

Contact person:
Leena Partanen, Study Monitor
tel +358 40 669 2853
e-mail: ext-leena.partanen (at) hus.fi

16.8.2017/kv

 
 

Monitoring service for investigator-initiated clinical studies

Clinical Research Institute HUCH Ltd offers monitoring services for investigator-initiated clinical studies. 

Regular quality control is performed according to the regulatory requirements, the principles of good clinical practice (ICH-GCP) and the standard operating procedure of Clinical Research Institute HUCH Ltd. The investigator can determine the level of needed quality control in the study.

The investigator should contact the study monitor in early stage when planning a clinical study. The level and nature of monitoring are determined separately for each study in a study specific monitoring plan.

Contact person:
Leena Partanen, Study Monitor
tel +358 40 669 2853
e-mail: ext-leena.partanen (at) hus.fi

16.8.2017/kv