Bringing Therapies to Patients When Standard Channels Fail

When the medicine a patient needs is unavailable, unlicensed locally, or in shortage, care can stall at the ward or dispensary window. We create compliant access pathways that deliver to hospitals, specialty centers, and pharmacies when no standard route exists. This includes coordinating the right pathway, assembling documentation, managing health authority interactions, and delivering temperature-controlled products with full traceability. Clinically justified requests move from prescription to confirmed site receipt, supporting access and continuity of therapy without compromising compliance or patient safety.

In the rapidly evolving healthcare landscape, access to essential medicines often faces regulatory and supply barriers. Our treatment access solutions establish compliant, patient-specific pathways that enable access to rare, niche, or unlicensed therapies, address temporary shortages, and support cross-border supply for clinically justified cases.

Our focus is innovative patient care and continuity. Dedicated case handling and visible status, paired with secure temperature-controlled delivery, help keep access on track. Coordinating with clinical teams and aligning with regulatory requirements removes practical barriers, so treatment can proceed without delay.

We remove operational obstacles,so treatment can proceed without delay, making sure innovative treatments reach the point of care when standard channels fall short, because getting therapy to the patients who need them is what matters most.

Our Treatment Access Solutions

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    Individual Import
    Patient-Specific Access to Non-Marketed Innovations. Expands care options with compliant access to innovative therapies approved outside the local market for clinically justified cases.
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    Shortage Resolution
    Restore continuity of care during supply disruptions. Proactive market scanning, authority collaboration, qualified alternatives, and controlled distribution to keep care sites supplied.
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    Regulatory Landscape Guidance
    Practical clarity on country-specific routes to treatment access. Hands-on enablement across countries: regulatory guidance to move cases from request to pharmacy receipt.
  • Patient-first, care-centric handling

    Single case owner, transparent status, and checklist documentation keep cases moving and care continuous.
  • Speed with certainty

    Bonded-warehouse release, established customs & OR workflows, and temperature-controlled last mile to hospital or pharmacy receipt.
  • Licensed global access network.

    Quality-assured sourcing with falsified-medicine safeguards, serialization, and end-to-end batch traceability.
  • Authority-aligned, multi-country enablement.

    Correct use of named-patient and shortage pathways, plus practical broker and IOR guidance as well as documentation support.
  • Proactive access insights.

    Continuous shortage and regulatory-approval monitoring, demand validation, and early qualification of alternatives to protect continuity of care.

“When a standard route isn't available, it's our job to find one that is”

Branded Drugs

Originator medicinal products approved for clinical use and protected by intellectual property rights.

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Generics

Medicinal products containing the same active substance as reference products and demonstrating bioequivalence following patent expiry.

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Orphan and Ultra-Orphan Drugs

Medicinal products developed for rare diseases affecting small patient populations, often supported by specific regulatory incentives.

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Biosimilars

Biologic medicines highly similar to approved reference biologics, with no clinically meaningful differences in safety, purity, or potency.

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Cell and Gene Therapy (ATMPs)

Advanced therapies based on genes, cells, or engineered tissues, including gene therapies, cell therapies, and tissue-engineered products. These therapies operate under specialised regulatory frameworks due to their complexity and transformative potential.

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Controlled Substances

Medicinal products subject to special legal controls due to risks of abuse, dependence, or diversion, requiring strict handling and documentation throughout their lifecycle.

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Veterinary Drugs

Medicinal products developed for the prevention, diagnosis, or treatment of diseases in animals, regulated separately from human medicines.

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Nutraceuticals

Products derived from food sources that provide health or wellness benefits beyond basic nutrition, including supplements and functional ingredients.

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Diagnostic Medical Devices

Devices and tests used to identify, stratify, or monitor patients before or during treatment, including companion diagnostics linked to specific therapies.

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Therapeutic Medical Devices

Medical devices delivering treatment through mechanical, physical, or digital means, used in both clinical and post-approval care settings.

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