QR coding and scanning under GMP standards to ensure accurate delivery of the right medication to the right patient.

Translation services, secondary packaging, label design, and generation of labels from single panel to complex booklet labels.

Our processes and facilities ensure complete tracking of every movement across facility areas (storage, intermediate zones, and cleanrooms) under secure and controlled environmental conditions.

Specialized clean areas with distinct temperature ranges and continuous monitoring of temperature and humidity to safeguard medication integrity.

Guaranteeing a secure product supply chain in accordance with EU GMP guidelines, including global third-party auditing.

Our experts certify batches for human use, offering clear guidance through the release process, even for the most complex advanced therapies.

Qualified Personnel (QP) available to provide hands-on expertise and guidance before trial startup.

Ensuring medication traceability, quality, and optimal shelf life of marketed products.

A meticulously planned and executed purchasing process to deliver authentic, non-counterfeit products for clinical trials.

Implementation of robust anti-counterfeit measures to prioritize patient safety.

Assisting sponsors in providing patients with access to unlicensed medicines through structured and compliant processes.

Optimizing the programme’s effectiveness to ensure seamless and efficient execution.

Solutions ranging from short-term to long-term biological sample storage.

LN2 vapor storage -20º and -86°C freezers for optimal preservation.

24/7 monitoring connected to a centralized alarm system to ensure sample integrity.

Secure backup environments for maintaining sample safety.

Easy data extraction and management in accordance with CFR21.11.

Controlled access and recovery systems to protect sensitive information.

Redundant storage systems to safeguard against potential data loss.