Protecting Patients, Safeguarding Data
What We Do
End-to-end monitoring services ensuring patient safety, data integrity, and regulatory compliance.
Our Expertise
– Risk-based monitoring: efficient and focused oversight.
– Experienced clinical monitors who have worked in local and international settings.
– Quick issue resolution pipeline.
– Regulatory quality in adverse event management and safety reporting.
– Oversight of informed consent, adverse event reporting, protocol adherence.
– Data query management, source document verification, corrective & preventive actions.
Client Journey
– Monitoring Plan – tailored risk-based strategy
– Baseline Checks – site readiness & compliance audit
– Ongoing Visits – continuous oversight & reporting
– Close-Out Monitoring – final compliance, CSR validation
Why Partner with Us
– Proactively avoid issues that could delay or compromise trials.
– Monitors with dual local & international trial experience
– Quick corrective action pipeline to avoid data loss
– Focus on patient safety at every step
– Transparent reporting system
Contact With Us
Request a monitoring proposal.