In today’s highly competitive clinical trial landscape, returns and destruction play a crucial role in ensuring regulatory compliance, data integrity, and patient safety. Proper handling of unused or expired investigational products and clinical supplies is essential to maintain trial transparency and adherence to global guidelines.
We manage the return of investigational products and clinical supplies in accordance with industry standards and sponsor requirements.
We ensure safe and compliant destruction of expired, damaged, or unused products following GxP, GMP, and local regulatory guidelines.
Our process includes detailed tracking and documentation, ensuring audit readiness and compliance with 21 CFR Part 11 regulations.
We follow eco-friendly destruction methods to reduce environmental impact.
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