Direct To Patient Distribution

Marken can guarantee the integrity of your clinical trial materials from any sponsor site to any patient, either from the sponsor site, the packager, or from any of our global depots.

Marken has the expertise you can rely on for distribution of your trial materials directly to patients. Once the patient information and schedule of drug deliveries are established, Marken does all of the necessary logistics planning and ensures that trial materials are properly packaged and delivered to the patient on-time and within spec.

Marken carefully controls the temperature profile of trial materials, allowing every patient to receive materials at their full efficacy. Marken depots can provide proper storage and distribution of materials at the temperature profiles required to maintain product integrity. All our depots have the ability to store and handle product at ambient, controlled ambient (15 – 25°C), cold storage (2-8°C), frozen (-20°C), and deep frozen (-80°C). The depot will also pick and pack materials for the trial, ensuring that the patient has everything needed to participate in the trial.

Shipments often cross international borders, but Marken has a deep understanding of international regulations and customs requirements. This may mean preclearance and/or prepayment of duties to expedite delivery. This level of competence means products move across borders as smoothly as possible.

The same skill sets necessary to move trial materials from a depot to a patient also apply to distribution of trial materials from an investigator site to a patient or from a sponsor site to a patient

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 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 trial materials or help investigator sites perform more effectively
• • Get reliable advice from trained supply chain and regulatory professionals