February 2020

With an emerging clinical trial ancillary supply chain, and little research into effective management models, it has never been more urgent for management systems to step up to an increasingly complex trial landscape. Today’s pharmaceutical landscape relies increasingly on outsourcing efforts. Meanwhile, global rules, laws, and regulations continue to evolve at a rapid pace, and pressure to expedite market approvals for new drugs mounts. Due to the intertwined factors, a new, extremely complex global ‘ancillary’ supply chain has emerged. In this era of change, how does the ancillary supply chain respond to the needs of a rapidly changing industry and create better outcomes for drug discovery organisations and their patients?
As published in International Clinical Trials Journal

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When a pharmaceutical client came to Joanne Santomauro nearly 15 years ago with a request to help with a complex and expensive ancillary supply challenge, she didn’t hesitate. She launched Ancillare and began the journey to create and revolutionize ancillary supply chain management for the clinical research industry. Ancillare, which is a certified woman’s owned business, offers dynamic clinical trials process management services, including ancillary and clinical supply management, regulatory compliance services, and global logistics management. “Pharma companies are looking for better, faster, less expensive ways to bring a new drug to market, ancillary supply is one piece of that equation,” Joanne says.
As published in PharmaVOICE

READY TO OPTIMIZE YOUR SUPPLY CHAIN?

Request a Complimentary Clinical and Ancillary Supply Review