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In cases where biopharmaceutical companies lack the bandwidth or expertise to get their innovative medicines approved in other countries, a Named Patient Program can make their medicines available internationally.

This process, a widely accepted practice for many pharmaceutical companies, enables healthcare professionals across the world to request new medicines, for patients who have no other treatment options available to them in their own countries.

As part of the Personal Importation Process, the patient submits all the necessary documentation, including passport and medical information, to make a request for a small amount of medicine.

We refer to our "Access as Services" program as "Tech-enabled Named Patient Program," and that means we not only handle the logistics of international shipment, custom clearance, storage and distribution, but also assist pharmaceutical companies in gaining market access that will generate early revenue for them, as well as provide them with the real-world evidence (RWE) necessary for local regulatory approval.

There are many advantages for biopharma companies with a newly approved medicine to discuss with us to set up a Named Patient Program:

- Managing unsolicited patient requests for drugs in an ethical and regulatory controlled manner

- Building a stronger network of KOLs and future advocates by exposing physicians in new markets to your products

- Providing benefits to patients suffering from conditions, including some that can be life-threatening.

- Generating additional revenues in countries that allow you to charge for drugs supplied on a named patient basis

- RWE acquisition based on Asian demographics which accounts for 25% of the world population

Companies can provide drugs to patients in any country in which they have not yet received marketing authorization.

This includes countries in which a company plans to seek marketing approval, as well as those countries in which a company does not plan to seek marketing approval.

With a properly established Named Patient program, we help navigate the complex regulatory landscape, especially in Asia countries, and manage the shipment, customs clearance, and delivery to treating clinics.

Asia is a huge, rapidly growing and attractive market that is hard to ignore. Building a reputable early entry program with a US-based partner with a significant local presence is essential.

We invite biotech and biopharma companies interested in helping more patients who have no access to your medicines, to contact us.

We can share introduction materials or schedule a demo to learn more about our full range of offerings.

With access to our in-house expertise and knowledge of international regulatory and legal frameworks in Asia, we will be able to help pharmaceutical companies gain market access which will not only generate early revenue for them but also provide them with real-world evidence (RWE) crucial to local regulatory approval.

In addition to relationships with top hospitals, KOLs and Government agencies, Medebound HEALTH also partners with largest rare disease consortium, and this year, signed an agreement to help their hundreds of thousands rare disease patients source the latest medicines –both approved and not-yet-approved.

In the past, we have successfully imported and supplied of unlicensed medicines in oncology, neurology and rare diseases into the Asian region. Please contact us to learn more.

Medebound HEALTH has established its brand presence in Asia by contracting with the Asia’s largest insurance firms, and global Fortune 500 companies. Its services have covered worldwide members touching millions of lives, bringing new hope to patients who would otherwise have to travel abroad for care.