Blinding, Repackaging & Labeling Support
'Ensuring precision, confidentiality, and compliance in every pack.'
Quantime provides comprehensive Blinding, Repackaging, and Labeling Support to ensure the confidentiality, accuracy, and regulatory compliance of clinical trial supplies. Our services are designed to maintain study integrity while meeting protocol-specific requirements and Good Manufacturing Practice (GMP) standards.
We understand that precise and compliant packaging plays a critical role in trial success. Through our qualified network of GMP-certified partners and in-house expertise, we manage the entire process — from strategy design to execution — ensuring consistency, traceability, and product security.
Our tailored Packaging and Labeling Solutions are designed to meet the specific needs of every clinical study
Our capabilities include:
Blinding & Randomization
Implementing single, double, or open-label strategies while preserving the integrity of trial data.
Repackaging & Relabeling
Customizing packaging configurations to meet specific protocol needs, patient kits, or regional labeling requirements.
Multi-language Labeling
Providing compliant, multi-language labels aligned with country-specific regulatory guidelines.
GMP-Compliant Operations
Ensuring all activities are performed in qualified facilities under strict adherence to global GMP and GDP standards.
Quality Control & Documentation
Comprehensive batch documentation and quality checks to ensure complete accuracy and regulatory readiness.
With a focus on precision and quality assurance, Quantime ensures that every clinical supply item is correctly blinded, labeled, and packaged — safeguarding study integrity and enabling smooth global trial execution.
Ready to Transform Your Product Packaging?
Let Quantime create packaging solutions that protect, promote, and comply.
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