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About Us

Your dedicated partner in ensuring clinical trial excellence through independent oversight

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Our Mission

To safeguard clinical trial integrity and accelerate medical breakthroughs by providing meticulous oversight that ensures compliance with FDA regulations and protects patient safety.

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Why Choose Pristine

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FDA Compliance Expertise

Deep understanding of 21 CFR Part 312 Subpart D requirements and ICH/GCP guidelines ensures your trial meets all regulatory standards.

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Real-Time Oversight

Hands-on approach with accompanied site visits (PSV, SIV, IMV & COV) provides immediate insights and risk mitigation.

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Experienced Team

Senior oversight professionals with extensive experience in clinical operations and regulatory compliance.

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Independent Oversight

Unbiased monitoring ensures objective assessment and protection of trial integrity.

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Risk Prevention Focus

Proactive identification and resolution of potential issues before they impact your trial.

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Partnership Approach

We integrate seamlessly with your team while maintaining independent oversight.

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We Are Committed To Your Clinical Trial Success As Well As Your Team AND Personal Success

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Ready to Ensure Your Trial's Success?

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Let's discuss how our experienced team can provide the oversight needed to protect your trial's integrity and ensure regulatory compliance.

Schedule A Consultation