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Study Monitoring

Compliance and data integrity are the key aspects reflecting the quality of clinical studies. To ensure compliance with relevant requirements and integrity of study data, continuing monitoring of clinical studies is needed.

Monitoring is the act of overseeing the progress of a clinical study, verifying the proper documentation and reporting of study data, and ensuring that the study is properly conducted by the investigators and other research personnel in accordance with the study protocol and other relevant requirements.

HKU-CTC has a team of qualified and experienced study monitors who are capable of performing professional monitoring – in Hong Kong or in the Asian region – in accordance with HKU-CTC’s SOPs (or the SOPs of sponsors/CROs as required). Any special event or finding identified at a study site will be reported promptly to the sponsor/CRO with practical solutions proposed.

Highlights
Qualified and experienced study monitors
Full compliance with in-house SOPs (or the SOPs of sponsors/CROs as required)
Familiar with local hospital environment, making monitoring more efficient
Experience in monitoring multicentre studies
Services available for industry-sponsored and investigator-initiated clinical studies – in Hong Kong and the Asian region