Out-licensing

Out-licensing, different options:

In addition to its CDMO services, Unither Pharmaceuticals offers other types of collaboration based on its technological platforms. We support your growth with flexible relationships to ensure your success in the marketplace. In the pharmaceutical industry, out-licensing allows companies to expand their market reach and product offerings by entrusting development and regulatory aspects to our CDMO. Our turnkey products enable partners to focus on marketing and distribution while we manage production and compliance.

 

Differentiate and expand your product range! Unither Pharmaceuticals offers pharmaceuticals and medical devices for diverse therapeutic needs, including ocular cleansing, inhalation, lubrication, rhinology, ophthalmology, ear care, cough and cold relief, oral health, fever and pain management, gastroenterology, and addictionology. Patient comfort and compliance are at the heart of our product development process. 

 

Ready to explore our out-licensing opportunities? Partner with Unither Pharmaceuticals for access to our expertise and resources, ensuring successful product launches. Either you want to develop or manufacture an existing or a new product, please contact us.

1- License
or transfer of MA

Following the development of in-house products and the compilation of the registration dossiers, we grant licenses on our MAs (marketing authorization) obtained either in DCP (decentralized procedure) or a national repository for a possible extension with a MRP (mutual recognition procedure) depending on market demands or the needs of our partners.

2- Sale of pharmaceutical
dossiers

We can also assign to our partners the rights to the dossiers ready to be submitted for the registration and marketing of products on their territories. Our dossiers ensure regulatory compliance and adhere to all essential regulations and guidelines, facilitating a smooth approval process.

3- Medical devices

In parallel to drugs with an existing MA, we also develop and offer medical devices certified by notified bodies within the European Community.

All our records, MAs, and medical device certifications are intended to be used under license throughout Europe, and in the rest of the world with some adjustments, based on requests from local health authorities.

Whatever the type of partnership set up, we ensure the exclusive production of licensed products, maintaining high standards of quality and consistency. Our dedicated manufacturing facilities are equipped to handle diverse production needs, ensuring timely delivery and reliable supply.

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