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Clinical Kitting: More Than Just Packing Boxes

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Why Investigator Sites Shouldn’t Order Ancillary Supplies

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Learn what Clinical Trial Supply services we offer, how our services are delivered, and how you can benefit from an Ancillare Partnership.

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Why Ancillare
Because we
…maintain a therapeutically representative portfolio across all phases and stages

…boast established relationships and on-the-ground expertise across 22 strategic depots

…cover all major geographies, with access to all global clinical trial sites

…provide in-house medical staff and dedicated project managers to consult on every project

…offer our services at scale, allowing sponsors and CROs to realize 30%+ cost savings
A TRUSTED BIOPHARMA PARTNER →

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GLOBAL REACH →
THERAPEUTIC & MEDICAL EXPERTISE →
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Sponsors, CROs and SMOs, fill out the brief questionnaire and we’ll connect you to our development team.
For general inquiries, please contact info@ancillare.com
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Medical Consulting for Ancillary Supplies in Clinical Trials

Guidance That Connects Protocol to Product

Ancillary supplies may not be investigational, but they are essential. Ancillare’s medical consulting services ensure every supply choice — from syringes to storage devices — is clinically appropriate, globally sourced, and aligned with your trial’s protocol.

Our in-house medical supply experts provides early input during planning and protocol review, working alongside supply chain and regulatory teams to identify the right products and mitigate risk before issues arise.

Built Into the Supply Chain, Not Bolted On

Unlike traditional sourcing vendors, Ancillare integrates medical consulting directly into our Clinical Trial Ancillary Supply Chain (CTASC) model. That means Sponsors and CROs benefit from:

  • Therapeutic-area-informed supply recommendations

  • Global product availability analysis

  • Clinical justification for substitutions or equivalents

  • Input on usability, compatibility, and safety at the site level

  • Proactive risk identification (e.g., cold chain sensitivities, storage challenges)

Why It Matters for Your Trial and Your Patient

A mismatched supply does not just delay a study — it can put patients at risk. Ancillare’s consultative approach helps ensure every supply and equipment delivered is appropriate for use, reducing variability and protecting both the trial and the individuals who rely on it.

Whether you are managing a rare disease study or scaling across regions, our medical supply consulting supports:

  • Safer drug administration

  • Fewer site-level issues

  • Regulatory confidence

  • On-time trial execution

    Let’s Get It Right — From the Start

    Ancillare helps Sponsors and CROs avoid costly mistakes and safeguard trial quality by bringing clinical insight to every supply decision.

    With our patient-centric focus, we own supply chain success, ensuring trials launch on time with no regulatory delays related to ancillary supplies, so sites are supported, Sponsors’ objectives are fully met, and up to 30% cost savings can be realized.

    Our portfolio is therapeutically diverse with extensive experience in the following areas:

    Cardiovascular

    Oncology

    Vaccines

    Endocrine and Metabolic

    Neuroscience

    Ophthalmology

    Women’s Health

    More About Our Therapeutic Expertise

    Ready to align your ancillary supply strategy with clinical and patient needs?

    Contact us to speak with our Medical Supply Consulting Team. 


    Ancillare

    Americas: +1 877.474.5656

    Europe: +31 20899 1756

    info@ancillare.com

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