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Biologics, 'cold chain' among key issues in clinical trials packaging

Fisher Clinical Services’ Global Cold Chain Director Alex Guillen discusses developments in clinical trials packaging, including sustainability and cost issues.

Alex Guillen, Director, Fisher Clinical Services’ Global Cold Chain
Alex Guillen, Director, Fisher Clinical Services’ Global Cold Chain

Packaging World:
Tell us about Fisher Clinical Services.

Alex Guillen:
Fisher Clinical Services has focused on the unique nuances of clinical trials for more than 25 years through its packaging and labeling (blinded and open label); storage, handling and distribution of ambient and cold chain clinical trial materials; import/export services (including Importer of Record capability in more than 25 countries); comparator sourcing and ancillary supplies sourcing; all the way through to returns and destruction of supplies. Our clients range from innovative biotech start-ups to the largest multinational pharmaceutical and biotech companies.

How do you differentiate clinical trials packaging vs commercial packaging?
Clinical trials packaging normally considers the blinding element, something not factored into commercial packaging. Another major difference is in the logistics and timing to get a drug to the patient. Commercial drug distribution can take weeks or months, while clinical trials can be in hours. In terms of packaging, one major change has been the increased demand for reusable shippers to distribute clinical supplies globally. The ultimate goal here is to reduce waste.

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Check out new technology from 2,500+ packaging & processing suppliers
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