Project Operations
Transitioning from research to real-world application, the Project Operations phase is pivotal. It focuses on ensuring that every aspect of production is perfectly aligned with rigorous standards, in order to perfectly prepare for clinical trials. This stage prepares treatments for their journey into clinical trials, backed by a steadfast commitment to excellence and compliance.
Process Alignment with GMP
Ensuring that our processes align with Good Manufacturing Practices (GMP) is foundational. This alignment guarantees that our products are consistently produced and controlled according to quality standards.
Scale Up
Transitioning from small-scale laboratory settings to larger production scales is critical. This scale-up involves optimizing our production processes to meet the demand of clinical trials without compromising quality.
GMP Manufacturing
Our facilities adhere strictly to GMP guidelines, ensuring that every product batch is uniform and in compliance with regulatory requirements that govern pharmaceutical manufacturing.
Secondary Packaging
The right packaging is essential not only for safety but also for compliance. Our secondary packaging solutions are designed to protect the product and ensure its integrity throughout the clinical trial process.
GMP Storage
Our state-of-the-art storage facilities maintain optimal conditions for preserving the quality and efficacy of the pharmaceuticals. GMP storage is critical for protecting these materials until they are ready for use.
We offer Clinical Trial Preparation Services in
Jura, Switzerland
With more than 6,000 sqm of facilities and more than 20 years of experience, Adragos Jura offers customized clinical manufacturing to support your therapeutic trials.
