Access Solutions
moving medicines with purpose
Tanner helps biopharma companies & healthcare providers deliver medicines to patients who need them most, regardless of geography, regulatory status, or market barriers.
In this section :
explore our Access Solutions.
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Making a locally unapproved drug available on a free-of-charge basis in a controlled, patient-by-patient basis where the drug may never be commercially available.
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Making a drug available on a free-of-charge basis for philanthropic reasons.
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Provide temporary commercial supply using product labeled for another country or manufactured by another company to bridge gaps.
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Sponsored Studies providing drug supply and distribution support for independently designed and conducted research studies, ensuring regulated access, proper handling and compliance.
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Supporting the importation, and ongoing supply of an approved product into a market, including logistics, warehousing, order fulfilment and regulatory compliance to enable broader access.
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Providing contracted product supply to governments, NGOs, or public health agencies through competitive tender processes.
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Maintaining free-of-charge supply to trial patients, enabling trial closure while fulfilling an obligation to continuing supply to patients.
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Maintain continuity of supply after loss of Marketing Authorization or voluntary withdrawal for commercial reasons.
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Deliver emergency, rapid-response supply during public health emergencies, natural disasters, or disease outbreaks in coordination with health authorities and NGOs.
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Making a locally unapproved drug available on a for-charge basis in a controlled, patient-by-patient basis.
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our approach.
value-added services.
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Strategic and tactical guidance at evaluation stage on all program types at product or portfolio level.
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Collection of patient-level safety and efficiency data to support regulatory filings, pricing and reimbursement negotiations, or generate market intelligence.
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Provision of an online platform for larger programs to facilitate program enrolment for HCPs and patients, processing drug orders, collecting real-world data, and capturing safety events.
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Regulatory guidance, artwork creation, label printing, and secondary labeling and packaging.
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Strategic and tactical analysis, actionable recommendations, and support in securing funding in for-charge programs.