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Ancillary Kitting: More than Just Packing Boxes

Ancillary Kitting: More than Just Packing Boxes

Sep 19, 2025 | Articles, Featured

Some Sponsors assume they can cut costs or gain flexibility by shipping ancillary supplies in bulk to investigator sites. While this may seem efficient, ancillary kitting is far more than a logistical task. It is a strategic function that directly impacts patient safety, data quality, and regulatory compliance.

When sites are left to pull supplies from bulk inventory for each patient visit, Sponsors risk delays, inconsistencies, and quality failures that can compromise trial timelines and outcomes. Without centralized expertise and infrastructure, “hunting and gathering” becomes a source of risk rather than a point of control.

Here’s why relying on sites to source ancillary supplies directly is not a best practice.

 

Kitting Is a Strategy, Not a Packing Task

Effective ancillary kitting begins long before any items are packed. It involves upstream protocol alignment, global regulatory knowledge, and precise inventory planning and end-to-end supply chain coordination.

This complexity demands more than a logistics vendor. It requires a partner with the infrastructure and expertise to execute kitting with accuracy and reliability.

A qualified ancillary kitting partner must be:

  1. GxP compliant, with established SOPs and ongoing quality audits
  2. Built for operational excellence and packaging integrity
  3. Experienced in country-specific import regulations and labeling standards

Ancillare meets all these requirements. Our regulatory and quality collaborate with Sponsors to ensure every kit meets trial- and country-specific requirements, reducing the risk of delays, noncompliance, and site burden.

Why Site-Assembled Kits Create More Risk Than Reward

When Sponsors ship bulk supplies to clinical sites for local assembly, they introduce uncontrolled variables that can derail the trial. Most clinical sites are not equipped or staffed to handle kit assembly onsite with the oversight and compliance required.

Common risks of site-assembled kits include:

  • Increased workload for site employees, distracting from patient care
  • Kit content variations that lead to protocol deviations
  • Improper storage or inventory handling, including expired supplies
  • Customs delays and rejections due to inaccurate documentation
  • Lack of visibility and tracking once supplies leave the Sponsor

What appears to be a flexible or cost-saving solution often leads to inefficiencies, compliance issues, and increased patient risk.

Strategic Kitting Begins with Purposeful Design

True strategic kitting aligns directly with protocol requirements, enrollment forecasts, and site-specific needs. At Ancillare, we bring structure and predictability to the process with:

  • Protocol-driven kit configurations, customized by region or visit
  • Demand planning based on real-time enrollment and usage data
  • Centralized inventory with GDP-compliant storage
  • On-demand kitting to support resupply or urgent site needs
  • Expert supply selection through our Medical Supply Consulting team
  • Global network and specialized teams versed in country-specific requirements

While one box might seem like it can hold everything, many items require unique handling or packaging, and not all supplies are compatible. Expiration tracking must also be carefully managed.

This integrated approach ensures that clinical sites receive the right supplies at the right time for the right patient — reducing waste, avoiding shortages, and eliminating overages.

Custom Ancillary Kits Built to Protocol, Not Pre-Packaged

No two clinical trials are alike, and neither are their ancillary supply needs. Ancillare designs and assembles fully customized ancillary kits tailored to protocol requirements, regional regulations, and patient visits.

We manage the full kit production and distribution process, leveraging our unmatched global network to deliver with speed, accuracy, and compliance. Our teams monitor both regional and global trends to help Sponsors anticipate challenges and build resilience into their supply plans.

By aligning each kit to the patient journey — not just a supply list — we ensure that clinical sites receive exactly what they need, when they need it, without unnecessary burden or waste.

Ancillare supports a wide range of kit types, including:

  • Ancillary Trial Kits
  • Blood Collection Kits
  • Nursing Kits
  • Patient Supply Kits
  • Site Support Kits
  • Lab Kits for Specimen Collection

As your single-source partner, we work collaboratively to implement flexible, scalable solutions — simplifying the complexity of clinical trial supply while increasing site efficiency and Sponsor confidence.

Kitting with Ancillare: A Strategic Advantage

Ancillary kitting is not a background task; it is a strategic component that can advance or delay your clinical trial. When done right, it brings clarity, consistency, and control to a complex global supply chain.

Working with Ancillare makes it easy to alleviate site burden through expertly sourced and assembled kits, built to your exact specifications and designed to support every aspect of the patient’s journey.

Ancillare is more than a service provider. We are a strategic partner, purpose-built to support Sponsors and CROs across the full clinical trial supply chain. Our kitting solutions are compliant, customizable, and aligned for global execution to help Sponsors move faster, reduce risk, and stay focused on clinical trial success

Ready to Elevate your Ancillary Kitting Strategy?

Partner with Ancillare to streamline trial execution and gain control over one of the most overlooked — yet critical — components of the clinical trial supply chain.
Contact Us for a Quote

Ancillare Enhances Cold Chain Management Services for Clinical Trial Supplies

Jan 29, 2025 | Press Release

HORSHAM, Pa. — January 29, 2025 Ancillare, the global leader in clinical trial supply chain solutions, is pleased to announce the launch of its state-of-the-art Cold Chain Management services, specifically designed to ensure the safe handling and transport of temperature-sensitive supplies and equipment in clinical trials.

Recognizing the critical nature of temperature-sensitive products in clinical research, Ancillare is committed to maintaining precise refrigerated temperatures throughout the entire supply chain. This new service offering extends beyond transportation; it includes sourcing of the item, customs clearances, monitoring product expiry, and providing robust inventory management. These features are designed to guarantee the highest standards of quality, integrity and efficiency throughout the supply chain.

“Our enhanced Cold Chain Management services are a testament to Ancillare’s commitment to innovation and excellence in the clinical trial supply chain,” said Dr. Joanne Santomauro, CEO at Ancillare. “By offering a fully integrated approach that covers every aspect of the process – from sourcing to handling, storage, and transportation – we ensure that all products remain in optimal condition, while meeting stringent global regulatory requirements. This enables our Sponsors to avoid delays and disruptions that could negatively impact clinical trials.”

Ancillare’s comprehensive cold chain services help Sponsors achieve significant cost savings, optimize resource allocation, reduce risks, and improve overall coordination throughout the supply chain.

For more information about Ancillare and its Cold Chain Management services, see our Services page or request more information.

About Ancillare
Ancillare is a full-service clinical trial supply partner that Life Sciences companies of all sizes, and at all development stages, rely on. From startup to closeout, and from supply sourcing to equipment reclamation and study disposition, we are the pioneers in clinical trial ancillary supply consulting and management, experienced in the full spectrum of clinical trial life cycle variables.

The Ancillare Team leverages extensive global buying power, a vast depot network, and subject-matter experts in research, procurement, operations, logistics, and regulatory matters to create tailored clinical supply and equipment programs for the most demanding Phase I-IV clinical research.

We help executives achieve better operational efficiency at all levels of the trial value chain. Simplifying and streamlining supply processes —that’s our specialty. Reduced costs. Expedited cycle times. Risk well-managed. The benefits are measurable, but the results are invaluable.

Clinical Trial Supply and Logistics Supplement: Quality assurance and regulatory compliance, and ancillary supply chain management

Clinical Trial Supply and Logistics Supplement: Quality assurance and regulatory compliance, and ancillary supply chain management

Aug 30, 2024 | Articles, Industry Publications

The evolution of the clinical trial ancillary supply chain (CTASC), the globalisation and expansion of clinical trials in the most difficult regions of the world, and the requirement for better, faster and leaner methods, have presented a myriad of unforeseen and unprecedented risks and challenges for the CTASC organisation. The CTASC professional must possess the ability to research, evaluate, execute and guarantee that all components and all links in the chain align to achieve success.

As published in International Clinical Trials: Clinical Trial Supply and Logistics Supplement

VIEW THE ARTICLE

Ancillare CEO Appointed to Serve on Supply Chain Management (SCM) Advisory Board at Temple University’s Fox School of Business

Aug 22, 2024 | Press Release

HORSHAM, Pa. — August 22, 2024 Ancillare, a global leader in global clinical trial supply chain solutions, proudly announces that Dr. Joanne Santomauro, Ancillare’s CEO, has been invited to serve on the Supply Chain Management (SCM) Advisory Board at Temple University esteemed Fox School of Business.

Joanne Santomauro brings over 40 years of experience in supply chain management and has been instrumental in the innovation and expansion of Ancillare’s Clinical Trial Ancillary Supply Chain (CTASC™) model. Since founding the company in 2006, Joanne’s leadership has propelled Ancillare to a prominent position in the global market.

Joanne holds advanced degrees, including a Doctorate in Business from the Temple University Fox School of Business. Her appointment to the SCM Advisory Board underlines Ancillare’s commitment to academic excellence and industry innovation.

Fox School of Business’s SCM program is renowned for its dynamic community of undergraduate and PhD students, guided by a faculty with nearly a century of collective industry experience. The SCM Advisory Board, consisting of supply chain executives from various industries, plays a crucial role in shaping the next generation of supply chain professionals.

“I am honored to serve as a board member for Fox School of Business’s SCM program”, said Dr. Joanne Santomauro. “As the demand for skilled supply chain professionals continues to grow, Fox School of Business is poised to be at the forefront of supply chain education and research.”

Dr. Santomauro’s expertise and leadership in clinical trial supply chain management will provide invaluable perspectives to the board, enhancing the curriculum and strengthening the bridge between academia and industry.

About Ancillare

Ancillare is the only full-service ancillary supply partner that Life Sciences companies of all sizes, and at all development stages, rely on. From start-up to closeout, and from supply sourcing to equipment reclamation and study dissolution, we are the pioneers in clinical trial ancillary supply consulting and management, experienced in the full spectrum of clinical trial life cycle variables.

The Ancillare Team leverages extensive global buying power, a vast depot network, and subject-matter experts in research, procurement, operations, logistics, and regulatory matters to create tailored ancillary supply and equipment programs for the most demanding Phase I-IV clinical research.

We help executives achieve better operational efficiency at all levels of the trial value chain. Simplifying and streamlining supply processes —that’s our specialty. Reduced costs. Expedited cycle times. Risk well-managed. The benefits are measurable, but the results are invaluable. To learn more, visit us at https://www.ancillare.com

To Research Faster, You Need an Ancillary Partner Who Reaches Further

To Research Faster, You Need an Ancillary Partner Who Reaches Further

Jul 30, 2024 | Articles

Bringing innovative therapies to the market involves more than sound science. It requires operational excellence in every step of the clinical trial journey to raise the probability of success.

Every clinical trial is unique. From protocol to therapeutic specialty to patient nativity, each trial has specific and unique needs. However, every clinical trial shares a common characteristic: the dependency on well planned processes to deliver on-time and on-budget studies.

At Ancillare, we develop leading global programs to manage the ancillary supplies that are critical to how far a clinical trial can progress and how fast it gets there.

Like IPs, Ancillary Delays Derail Clinical Research

Ancillare–the leader in ancillary supplies and equipment management programs–calculates that Sponsors could achieve over 30% in cost savings by optimizing how they manage their trial’s ancillaries.

Sponsors spend a lot of energy and resources coordinating the efficient sourcing and regulatory requirements of the clinical side of the trial.

However, the truth of trials is that both a biosimilar and a portable refrigerator can bring a clinical trial to a halt. And send budgets and timelines spiraling.

Even minor oversights in ancillary supplies can prevent or delay revolutionary therapies from reaching the patients they were developed to help.

Trials truly built to accelerate research and expand global treatment delivery demand expert management of every detail of the trial process. And the most significant of the overlooked details is often ancillary supplies and equipment.

There Are No Small Parts in Clinical Trials

Clinical trials require the alignment of many moving parts. If one of them stops, two things tend to happen: timelines extend and costs rise.

Ancillary supplies and equipment programs provide an excellent illustration of how Sponsors can lose time and money by leaving some components of their trials unattended, or poorly planned and managed.

Supply Chain Gaps Cost Sponsors Millions

Ancillaries–every non-drug item needed to execute a trial–represent about 4.2% of a clinical trial’s cost. On average that means anywhere from $168k-$840k at the outset of the trial. May not sound like a significant upfront line item, but a lack of management and subsequent delays cost upwards of $600k/per day (with estimates as high as $8MM).

Managing ancillaries requires skills that demand extraordinary levels of competence in logistical coordination, sourcing, transnational relationships, risk and project management.

Sponsors and CROs rightly spend the majority of their supply chain focus on the IP itself. But without a specialized skill set around ancillaries and equipment, they end up paying higher prices for ancillary items and incurring increased freight, storage, reclamation, and disposition expenses. Compounded upon that is the constant juggling of regulatory and coordination intricacies that require import/export expertise and on-the-ground experience in the countries and at the sites where trials are being conducted.

Together, these gaps and inefficiencies lead to delays, significant increases in goods and equipment costs, and additional management fees to handle rush issues. Sponsors and CROs can quickly see budgets and timelines spiral out of control.

Prevention’s Power: Reach Further and Research Faster

Ancillare has dedicated the last 17 years to making clinical trials happen in over 100 countries – collaborating with Sponsors to address and relieve their unique pain points while developing tailored plans that acknowledge prevention as the best medicine.

Ancillare’s work is grounded in partnership. Not just with the Sponsors who trust us with their trials’ ancillary supply and equipment programs, but also across the globe and throughout our extensive strategic depot network. The difference maker for Sponsors and CROs alike is our hands-on approach in both the planning and the operational execution of their programs.

Our full service partnerships include:

  • Protocol analysis to anticipate supply and equipment needs.
  • Medical consulting to mitigate risk of item availability and/or regulatory issues.
  • Single-source model with 22 strategic global depots.
  • Import/export management facilitating trials’ requisitions.
  • Returns, reclamation, and disposition services to support closeout requirements.

Ancillary supply and equipment programs are a strategic investment, not an expense. Taking a patchwork, ad hoc approach, or figuring things out along the way, can and will result in hidden costs and vital days lost for patients’ access to life-improving treatments.

Schedule a consultation today, and let’s keep your research moving forward.

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