Clinical Monitoring

Our highly trained, expert and safety-oriented clinical research professionals provide clinical trial monitoring services that are tailor-made to our clients’needs. Our clinical trial monitoring team support:

• Site identification and selection, performing on-site or remote pre-study visits
• On-site or remote site initiation, interim and close-out monitoring visit activities
• Verify the rights and wellbeing of clinical study’s participants are protected
• Confirm consent, eligibility, safety and data integrity
• Training of investigational site staff
• Informed consent/document translation, verification and back-translation
• Preparation of regulatory or ethics/review board submissions
• Timely submission of protocol/consent and other documents
• The storage of drugs, management of intellectual property and clinical study materials
• Reporting of protocol deviations
• Regular reporting.

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