Therapeutic Supply Chain
At the heart of Marken’s therapeutic supply chain is a network of strategically located, purpose-built depots. We currently support trials at over 49,000 investigator sites around the globe.
Marken provides the expertise, experience, and resources to help pharmaceutical and life science companies conduct their clinical trials in an effective and efficient manner.
At the heart of Marken’s therapeutic supply chain is a network of strategically located, purpose-built depots. We currently support trials at over 49,000 investigator sites around the globe. Our services ensure that your products receive proper packaging, distribution, storage, and handling at every step in the process.
Our management is made up of pharmaceutical industry experts who understand the critical need to maintain the required temperature profile of your drug or device. Whether in transit or in storage at our depot, Marken has the capability of continuously maintaining your product at controlled ambient, cool chain, cold chain, deep frozen, or LN2.
When moving your drugs or devices across country borders, Marken’s expertise and in-depth knowledge of the regulatory environment for the pharmaceutical industry will help you ship your product anywhere in the world. This knowledge and expertise helps ensure rapid movement through customs, minimizing potential loss of product on its way to an investigator site.
Every Marken facility is GMP-compliant, and at every step in our business processes, we apply quality management principals.
With Marken, the responsibility of storage, packaging and logistics are removed from trial sites, allowing pharmaceutical company personnel to concentrate on management of the trial itself.
Marken’s just-in-time delivery of clinical trial materials to sites or even individual patients means smoother and more efficient conduct of trials, even in remote locations. For a supply chain that works, Marken makes it happen.
- Ongoing global access to the status of your inventory and shipments gives you visibility and control
- Conduct trials in more remote locations with greater access to clinically naïve patient populations
- Eliminate your investigators’ storage and logistics concerns for specimens, controlled substances or time and temperature-critical materials
- Get reliable advice from trained supply chain and regulatory professionals