Return & Destruction Services
'Secure Returns. Compliant Destruction.'
Quantime provides fully compliant Return and Destruction Services for investigational medicinal products (IMPs), comparators, and ancillary supplies at the end of a clinical trial or study phase. Our processes are governed by stringent Good Distribution Practice (GDP) and Good Manufacturing Practice (GMP) standards, ensuring accountability, traceability, and environmental responsibility throughout each step.
We understand the critical importance of proper reconciliation, documentation, and compliance in managing unused or expired trial materials. Through our global network and controlled operations, we ensure that all returns and disposals are executed in a secure, transparent, and regulatory-compliant manner.
Our services include:
Return Coordination
End-to-end management of IMP and ancillary material returns from clinical sites, ensuring accurate inventory reconciliation and documentation.
Inspection & Verification
Comprehensive verification of returned products, including batch numbers, quantities, and condition assessments before disposal.
Secure Storage & Handling
Temporary storage of returned materials under validated, temperature-controlled conditions until final disposition.
Destruction Management
Environmentally responsible destruction through authorized vendors in compliance with local and international regulations. We operate in full compliance with the rules and regulations set forth by regional government authorities.
Documentation & Certification
Complete audit trail and destruction certificates to meet sponsor and regulatory authority requirements.
Risk & Compliance Oversight
Strict adherence to GDP, GMP, and environmental safety standards to ensure accountability and transparency.
Key Features & Benefits
Compliance Management
Full adherence to GxP, GMP, and global regulatory standards.
Expert Team
Experienced professionals with deep regulatory knowledge.
Secure Transportation
Safe handling and transport of products for return/destruction.
Global Coverage
Services available across multiple regions and jurisdictions.
By maintaining full traceability and regulatory alignment, Quantime ensures that all returned and expired clinical materials are managed with the highest level of integrity—protecting study data, patient safety, and environmental standards while upholding sponsor confidence.
Ready to Ensure Compliant Returns & Destruction?
Let Quantime handle your clinical trial returns and destruction with the highest standards of compliance and security.
Get Started Today