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Ancillare Joins Decentralized Trials & Research Alliance (DTRA)

Feb 8, 2022 | Press Release

Leading life sciences supply chain organization promotes adoption of decentralized clinical trials alongside fellow industry leaders.

Horsham, Pa. — February 8, 2022. Global Clinical Trial Ancillary Supply Chain (CTASC™) leader Ancillare, LP, the first and only Life Sciences company dedicated to Ancillary Supply Chain for Phase I-IV clinical research, announced today it has joined the Decentralized Trials & Research Alliance (DTRA), an historic alliance of over one hundred life sciences and healthcare organizations that seeks to accelerate the broad adoption of patient-focused, decentralized clinical trials and research.

The “Decentralized Trials & Research Alliance (DTRA),” which launched December 2020, is uniting industry stakeholders, including healthcare companies, regulators, patient groups and research organizations with a singular mission to make clinical trial participation widely accessible by advancing policies, research practices and new technologies in decentralized clinical research.

“Decentralized trials are the future of clinical research, and a well-managed supply chain is foundational to their success,” said Dr. Joanne Santomauro, Chief Executive Officer, Ancillare. “As a member of the DTRA, Ancillare will help pave the way to broader adoption of decentralized trials through awareness and innovation of the global Clinical Trial Ancillary Supply Chain.”

“We are extremely gratified to welcome Ancillare to the ‘Decentralized Trials & Research Alliance,’” said Amir Kalali, MD, founder of several collaborative life science communities, and co-Chair of DTRA. “By advancing decentralized research we can make the clinical trial process more patient-focused, increase trial efficiency and encourage use of technologies. We are excited by Ancillare’s commitment to embracing decentralized trials and to changing the culture that has been the rate limiter to innovation.”

During the COVID-19 pandemic, Ancillare devoted greater focus to its Direct-to-Patient operation, which encompasses the assembly of ready-to-distribute single patient kits needed for decentralized research. The company is now expanding its facilities to accommodate enhanced kitting services for Sponsors conducting decentralized trials.

“Now is the time to share ideas and insights that will chart the future course of clinical trials, accelerating drug development and saving lives – and by taking part in the DTRA, Ancillare is demonstrating its leadership to drive change,” said Craig Lipset, DTRA co-Chair, clinical innovation advisor, and a pioneer in decentralized trials. “We have a responsibility to advance the health of people with unmet medical needs, and by convening stakeholders from pharma companies, regulators, technology leaders and patient communities, we can remove remaining barriers to adoption and impact patients today.”

To learn more about Ancillare’s work to advance clinical research through integrated supply chain strategies, visit Ancillare.com.

About Ancillare, LP
Ancillare is the first and only Life Sciences company dedicated to Clinical Trial Ancillary Supply Chain (CTASC™) for Phase I-IV clinical research. Ancillare arms Sponsors of global clinical trials with customized, end-to-end supply plans, enabling developers of new therapies to optimize their supply chains using streamlined processes, extensive global buying power, a vast depot network, and proven teams of clinical, procurement, operations, logistics and regulatory experts. Ancillare’s industry-shaping model navigates the complexities of the Clinical Trial Ancillary Supply Chain to reduce both the overall cost and cycle time of clinical trials, and greatly improve operational efficiency across all levels of the value chain.

Ancillare has supported more than 4,000 clinical trials across 200,000 clinical sites over 100 countries with corporate offices in the United States and the Netherlands, and distribution hubs in Argentina, Brazil, Canada, China, Israel, Japan, South Korea, Mexico, Netherlands, Philippines, Russia, Taiwan, and Ukraine. To learn more, visit Ancillare.com.

About DTRA
The Decentralized Trials & Research Alliance (DTRA) was convened to enable collaboration of stakeholders to accelerate the adoption of patient-focused, decentralized clinical trials and research within life sciences and healthcare through education and research. It works to make research participation accessible to everyone, enabled by the consistent, widespread adoption of appropriate decentralized research methods. Follow DTRA on Twitter and LinkedIn for more information.

Ancillare Purchases Property Within U.S. Pharma Hub, Begins Facility Renovation

Nov 9, 2021 | Press Release

Industry leader in Clinical Trial Ancillary Supply Chain announces plans to upgrade its headquarters in time for the new year

Horsham, Pa. — November 9, 2021. Global Clinical Trial Ancillary Supply Chain (CTASC™) leader Ancillare, LP, the first and only Life Sciences company dedicated to Ancillary Supply Chain for Phase I-IV clinical research, recently announced its purchase of office and warehouse space at 700 Enterprise Road in Horsham, Pennsylvania.

Strategically located in Greater Philadelphia, the new property is the second location owned by Ancillare within the pharma corridor of the northeastern United States. The company plans to renovate the space to accommodate expansion of its core capabilities, including kitting, labeling, and Direct-to-Patient operations. Initial upgrades to the office and warehouse facilities will be completed this year.

“As a partner to a number of the top global pharmaceutical companies, we are proud to continue building our physical infrastructure here in the Philadelphia area,” said Dr. Joanne Santomauro, Chief Executive Officer. “We are hard at work developing specialty services to address the unique challenges of the pandemic and its indelible impact on the global CTASC.”

In addition to its United States presence, the organization has a vast Global Distribution Network spanning North and South America, Europe, and Asia-Pacific, including a second headquarters in the Netherlands. For the most up-to-date information on Ancillare’s expansion efforts, visit Ancillare.com.

About Ancillare, LP

Ancillare is the first and only Life Sciences company dedicated to Clinical Trial Ancillary Supply Chain (CTASC™) for Phase I-IV clinical research. Ancillare arms Sponsors of global clinical trials with customized, end-to-end supply plans, enabling developers of new therapies to optimize their supply chains using streamlined processes, extensive global buying power, a vast depot network, and proven teams of clinical, procurement, operations, logistics and regulatory experts. Ancillare’s industry-shaping model navigates the complexities of the Clinical Trial Ancillary Supply Chain to reduce both the overall cost and cycle time of clinical trials, and greatly improve operational efficiency across all levels of the value chain.

Ancillare has supported more than 4,000 clinical trials across 200,000 clinical sites over 100 countries with corporate offices in the United States and the Netherlands, and distribution hubs in Argentina, Brazil, Canada, China, Israel, Japan, South Korea, Mexico, Netherlands, Philippines, Russia, Taiwan, and Ukraine. To learn more, visit Ancillare.com.

Ancillare Expands Sourcing and Export Capabilities to Include Medicinal Products

Sep 23, 2021 | Press Release

Leading life sciences supply chain organization acquires NG BV, a Netherlands-based company authorized to procure, supply, and export medicinal products.

Horsham, Pa. — September 23, 2021. Global Clinical Trial Ancillary Supply Chain (CTASC™) leader Ancillare, LP, the first and only Life Sciences company dedicated to Ancillary Supply Chain for Phase I-IV clinical research, today announced its acquisition of NG BV in the Netherlands.

As a company with a Wholesale Distribution Authorization (WDA), NG BV will market, procure, supply, and export medicinal products. The acquisition deepens Ancillare’s supply chain capabilities in the medicinal products space, allowing even greater control and supply chain transparency for Sponsors globally.

“The purchase of NG BV is a significant milestone for our organization,” said Dr. Joanne Santomauro, Chief Executive Officer. “The ability to manage medicinal products that facilitate clinical trials reinforces our position as a single-source partner for CTASC management and significantly supports the industry-unique Ancillare Turn-Key Operation (A-TKO™).”

Cathy Porretti, Chief Global Operation Officer, added: “We know many Sponsors value single vendor relationships to ensure smooth, timely trials. And through this acquisition and expansion, we are able to bring our proven methodology to another key part of the trial’s lifecycle.”

In the coming months, more expansion efforts will take place to strengthen Ancillare’s global supply chain infrastructure and service offering. For the most up-to-date information on Ancillare’s CTASC capabilities, visit Ancillare.com.

About Ancillare, LP
Ancillare is the first and only Life Sciences company dedicated to Clinical Trial Ancillary Supply Chain (CTASC™) for Phase I-IV clinical research. Ancillare arms Sponsors of global clinical trials with customized, end-to-end supply plans, enabling developers of new therapies to optimize their supply chains using streamlined processes, extensive global buying power, a vast depot network, and proven teams of clinical, procurement, operations, logistics and regulatory experts. Ancillare’s industry-shaping model navigates the complexities of the Clinical Trial Ancillary Supply Chain to reduce both the overall cost and cycle time of clinical trials, and greatly improve operational efficiency across all levels of the value chain.

Ancillare has supported more than 4,000 clinical trials across 200,000 clinical sites over 100 countries with a corporate office in the United States, and distribution hubs in Argentina, Brazil, Canada, China, Israel, Japan, South Korea, Mexico, Netherlands, Philippines, Russia, Taiwan, and Ukraine. To learn more, visit Ancillare.com.

Ancillare, a Tier 1 Diversity Supplier, Sponsors DCAT 2021 Women’s Virtual Networking Breakfast

Ancillare, a Tier 1 Diversity Supplier, Sponsors DCAT 2021 Women’s Virtual Networking Breakfast

Mar 24, 2021 | Press Release

Ancillare, a woman-owned business serving top global biopharmaceutical companies, will sponsor the annual women’s networking event on March 24.

Horsham, Pa. — March 24th, 2021. Global Clinical Trial Ancillary Supply Chain (CTASC™) leader Ancillare, LP, the first and only Life Sciences company dedicated to Ancillary Supply Chain for Phase I-IV clinical research, is proud to sponsor the DCAT Women’s Networking Breakfast on Wednesday, March 24.

Ancillare, a woman-owned business by the Women’s Business Enterprise National Council (WBENC), is proud to sponsor the event, which is presented annually by DCAT’s Alliance for Industry Women Committee. This year, the event features keynote speaker Erica Dhawan, CEO and Co-Founder of strategy consulting company Cotential. During the live presentation, Dhawan will speak about effective collaboration as discussed in her book “Get Big Things Done: The Power of Connectional Intelligence,” highlighting the skills needed to build stronger organizational cultures. Participants will learn how to solve problems and drive innovation by applying Connectional Intelligence (CxQ) to communication in the digital age.

“As a woman-owned business, Ancillare has a unique opportunity — and responsibility — to support women’s advancement in healthcare and pharmaceuticals,” said Dr. Joanne Santomauro, Chief Executive Officer. “We are proud to sponsor an event that promotes the power of engaged teams and innovative mindsets, which have been foundational to Ancillare’s growth.”

The Women’s Networking Breakfast, typically held during DCAT Week in New York City, is a members-only event for women in the pharmaceutical industry. This year, the virtual session will feature digital networking opportunities and a live Q&A with Dhawan.

Further details about the DCAT Women’s Networking Breakfast are available at https://dcat.org/wnb.

About Ancillare, LP
Ancillare is the first and only Life Sciences company dedicated to Clinical Trial Ancillary Supply Chain (CTASC™) for Phase I-IV clinical research. Ancillare arms Sponsors of global clinical trials with customized, end-to-end supply plans, enabling developers of new therapies to optimize their supply chains using streamlined processes, extensive global buying power, a vast depot network, and proven teams of clinical, procurement, operations, logistics and regulatory experts. Ancillare’s industry-shaping model navigates the complexities of the Clinical Trial Ancillary Supply Chain to reduce both the overall cost and cycle time of clinical trials, and greatly improve operational efficiency across all levels of the value chain.

Ancillare has supported more than 4,000 clinical trials across 200,000 clinical sites over 100 countries with a corporate office in the United States, and distribution hubs in Argentina, Brazil, Canada, China, Israel, Japan, South Korea, Mexico, Netherlands, Philippines, Russia, Taiwan, and Ukraine. To learn more, visit Ancillare.com.

Ancillare Receives Medical Device Establishment License in Canada

Jan 14, 2021 | Press Release

Ancillare, the industry leader in Clinical Trial Ancillary Supply Chain (CTASC™), obtains authorization to distribute medical devices in Canada.

Horsham, Pa. — January 14th, 2021. Global Clinical Trial Ancillary Supply Chain (CTASC™) leader Ancillare, LP, the first and only Life Sciences company dedicated to Ancillary Supply Chain for Phase I-IV clinical research, announced it obtained its Medical Device Establishment License (MDEL) in August of 2020 and is now actively importing medical devices in support of Phase I-IV clinical trials.

The MDEL, which allows for the import and sale of medical devices, will serve to strengthen Ancillare’s global distribution network.

Ancillare applied for the MDEL in response to the Canada Border Services Agency’s (CBSA) Single Window Initiative, which enacted new licensing requirements for importers of medical devices and other goods under Health Canada jurisdiction. The license demonstrates compliance to Health Canada’s Medical Device Regulation (MDR), and gives Ancillare the ability to import registered medical devices for clinical use in Canada.

“With an MDEL, Ancillare can better support our Sponsors by facilitating medical device imports,” said Dr. Joanne Santomauro, Chief Executive Officer. “Maintaining regulatory knowledge and compliance is among our key value offerings, and represents just one example of our ongoing efforts to strengthen Ancillare’s global distribution capabilities.”

To learn more about Ancillare’s service offering, including global distribution and regulatory support, visit Ancillare.com/Services.

About Ancillare, LP
Ancillare is the first and only Life Sciences company dedicated to Clinical Trial Ancillary Supply Chain (CTASC) for Phase I-IV clinical research. Ancillare arms Sponsors of global clinical trials with customized, end-to-end supply plans, enabling developers of new therapies to optimize their supply chains using streamlined processes, extensive global buying power, a vast depot network, and proven teams of clinical, procurement, operations, logistics and regulatory experts. Ancillare’s industry-shaping model navigates the complexities of the Clinical Trial Ancillary Supply Chain to reduce both the overall cost and cycle time of clinical trials, and greatly improve operational efficiency across all levels of the value chain.

Ancillare has supported more than 4,000 clinical trials across 200,000 clinical sites over 100 countries with a corporate office in the United States, and distribution hubs in Argentina, Brazil, Canada, China, Israel, Japan, South Korea, Mexico, Netherlands, Philippines, Russia, Taiwan, and Ukraine. To learn more, visit Ancillare.com.

Ancillare Appoints Dr. Georgia Crozier to Medical Director

Nov 12, 2020 | Press Release

Philadelphia-based optometrist Dr. Georgia Crozier joins Ancillare, leader in Clinical Trial Ancillary Supply Chain™, to consult on clinical trial planning.

Horsham, Pa. — November 12th, 2020. Global Clinical Trial Ancillary Supply Chain (CTASC™) leader Ancillare, LP, the first and only Life Sciences company dedicated to Ancillary Supply Chain for Phase I-IV clinical research, today announced it has appointed Georgia Crozier, OD, MS as a Medical Director to serve on its growing Clinical Development Team.

Dr. Crozier will leverage years of experience at multiple clinical sites to serve as a Subject Matter Expert for clinical trial planning and execution. Working directly with Ancillare’s internal teams and with Sponsors, Dr. Crozier will consult on matters of compliance for robust CTASC design.

An optometrist who has worked at a number of clinical sites, Dr. Crozier brings over 35 years of experience in her field —as a clinical investigator, medical consultant, and lecturer. She is a graduate of Pennsylvania College of Optometry at Salus University, and currently serves as the Director of the Moore Eye Institute Vision Rehabilitation Center.

“We are thrilled to bring on Dr. Crozier as a Medical Director,” said Dr. Joanne Santomauro, Chief Executive Officer. “Expanding our Clinical Development Team will further streamline the selection of ancillary supplies that meet increasingly demanding protocols and ever-changing global regulations. Ophthalmologic studies tend to be highly specialized with a broad range of supply and equipment needs, and we are excited to have Dr. Crozier’s expertise in-house for our Sponsors and clients.”

Dr. Crozier will serve as Medical Director alongside Dr. John Fitzgerald, who was recently appointed to the same role. The two physicians will work as a team and leverage their individual areas of expertise to better serve Ancillare’s Sponsors.

To read full biographies of Ancillare’s Medical Directors and learn more about the company’s Subject Matter Experts, visit https://www.ancillare.com/about/#leadership.

About Ancillare, LP
Ancillare is the first and only Life Sciences company dedicated to Clinical Trial Ancillary Supply Chain (CTASC) for Phase I-IV clinical research. Ancillare arms Sponsors of global clinical trials with customized, end-to-end supply plans, enabling developers of new therapies to optimize their supply chains using streamlined processes, extensive global buying power, a vast depot network, and proven teams of clinical, procurement, operations, logistics and regulatory experts. Ancillare’s industry-shaping model navigates the complexities of the Clinical Trial Ancillary Supply Chain to reduce both the overall cost and cycle time of clinical trials, and greatly improve operational efficiency across all levels of the value chain.

Ancillare has supported more than 4,000 clinical trials across 200,000 clinical sites over 100 countries with corporate office in the United States, and distribution hubs in Argentina, Brazil, Canada, China, Israel, Japan, South Korea, Mexico, Netherlands, Philippines, Russia, Taiwan, and Ukraine. To learn more, visit Ancillare.com.

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