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Regulatory Affairs Support
With clinical trials taking place in more than 200 countries worldwide, navigating the diverse and ever-changing global regulatory landscape simply isn’t feasible without the guidance of an expert logistics partner.
Global Compliance Experts
Yourway has more than 20 years of experience distributing highly sensitive biopharmaceutical goods and clinical trial materials across all continents, affording us an innate understanding of global regulations and the agility to adapt to changing requirements at both regional and local levels. Prior to origination, your dedicated project manager will coordinate with our operations teams to develop a logistics strategy that takes into consideration your product profile as well as region-specific import requirements to mitigate the risk of noncompliance and prevent costly delays.
Through our depth of experience, regulatory agency relationships and ongoing industry research, we are continuously monitoring changes that could impact the movement of our customers’ materials, employing a proactive approach to ensure each shipment is delivered to the intended destination safely and efficiently – without interruption.
Regulatory Affairs Capabilities
- Regulatory affairs consulting
- Customs clearance support
- Dangerous goods classification, preparation and documentation support
- Packaging and labeling compliant with regional regulations
The At-home Trial Experience: Leveraging value-chain to reach and retain patients
Import of Record (IOR)
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Discover how our global supply chain expertise and integrated solutions can enhance your clinical research.