MAKING HEALTHCARE ACCESSIBLE

HOW WE DO

Within initiating an early-phase I study, we care about proof of concept, efficacy, and stability of the patient within the shortest timeframe possible. Our dedicated services and tools in our global facilities enable state of the art performance while ensuring time and cost savings for our customers. Our team supports every step such as site selection, study design, and efficient IMP kit design to cover a flawless phase I performance.

• Dedicated Project Manager and coordinating with research centers.
• QP and regulatory services.
• Sourcing ancillaries, co-therapy and emergency medication.
• Fill and Finish of IMP.
• Primary and secondary packaging.
• Logistics and distribution to research centers.

HOW WE DO

We support phase II/III trials with a complete integrated supply chain, managing global sourcing strategies, packaging and distribution services, documentation support and risk mitigation strategies. Our dedicated team over a global presence covering all time zones through our centers of excellence to ensure a 24/7 support.

• Project Management services.
• Regulatory expertise and market intelligence.
• Strategic comparator, co-therapy, and ancillary procurement.
• Label design and translations.
• Primary and secondary packaging.
• Integrated Storage, Distribution and logistics management.
• Real-Time tracking and multi-site inventory management.

HOW WE DO

Our services for early access programs enable pharmaceutical companies to offer cutting-edge treatments to patients ahead of market approval. We manage regulatory compliance, patient eligibility, and program logistics, ensuring a seamless and efficient process.

• Project Management and coordinating with HCPs.
• Strategic planning for expanded or extended access programs.
• Streamlined regulatory compliance and patient eligibility management.
• Efficient program logistics ensuring timely access to treatments.
• Generation of valuable real-world data for informed decision-making.

HOW WE DO

We offer strategic pathways to provide patients with pre-approval access to innovative treatments. We handle regulatory compliance, patient eligibility, and program logistics to ensure smooth and effective implementation.

• Project Management and coordinating with HCPs and patients.
• Regulatory compliance tailored to regional imports.
• Seamless logistical support ensuring timely access to treatments in diverse regions.
• Import permits and regulatory submissions.

HOW WE DO

Our patient access programs enable pharmaceutical companies to provide lifesaving treatments in regions where products are not yet registered. We facilitate seamless distribution to doctors, patients, hospitals and government organizations, ensuring compliance with local regulations and efficient delivery. We accelerate access to critical therapies, supporting the health of patients by entering new markets.

• Efficiently manage the delivery of lifesaving treatments to patients and supporting treating parties.
• Ensure adherence to local regulations.
• Provide rapid access to critical therapies for patients in need.
• Managing treatment funding with health insurance and government organizations.
• Full logistics and import clearance support.