Clinical Trials supply chain and logistics activities may be challenging due to a variety of factors within the nature of this sector and the requirements they entail.
Among these constraints are the immaculate compliance with various regulatory standards, which may change; the unpredictability of patient enrollment, which requires providers of pharma logistics services like Movianto to be flexible and quickly adjust their supply chains. The worldwide scope of clinical trials, requiring compliance and navigation through various import/export regulations and modes of shipping or sometimes a need to custom supplies to unique trial protocols. Also, there are many other critical factors requiring close attention, including potential drug shortages and the consequent need for forecasting and inventory management.
All these pressures emphasise the need for a robust and flexible clinical trials supply chain, such as we have built at Movianto over decades of experience in the area.
When dealing with various demands our Clincial Trials Supply Department teammates are involved in all aspects of clinical trials logistics services: storage, secondary labelling, labels design and translation, distribution, process development, and beyond. Our specialists are committed to finding solutions together with our customers thereby building closer relationship with them.
We seek to continuously upgrade our knowledge and stay on top of legislation and the latest developments in the pharmaceutical world. Our vigilant approach to risk management and documentation is a commitment to patient safety, regulatory compliance and successful clinical trials operations.