Private label manufacture and out-licensing: Biofarma Group’s consolidated experience in ready-to-market products
Our market trend analysis expertise and know-how, combined with on-going partnerships with leading research centres, have allowed us to develop medical devices that we produce under private label manufacturing and out-licensing agreements.
These products are an embodiment of our vocation to developing highly-innovative products that guarantee our clients success.
Our medical devices:
- pertain to MD classes I, IIa, IIb and III
- are intended for use in a range of therapeutic areas
- have solid and liquid forms
- are for internal oral and topical use
- are manufactured in ISO 13485-certified facilities
Third-party manufacturing of medical devices
At Biofarma Group, we provide our clients with a turnkey service, from analysing their needs through to satisfying their demands and making their market presence unique.
We offer and deliver innovative solutions for all therapeutic areas: from the gastrointestinal and metabolic area to personal hygiene, from baby care to skin care, from cough and cold to allergies, through to feminine hygiene and the proctology area.
Third-party manufacturing of medical devices: the therapeutic areas
Out-licensing medical device manufacture
We manufacture more than 70 ready-to-market products, many of which are patented. We oversee every stage of the process, from formulation to development, through to the supervision of all aspects of product certification, including biocompatibility testing, stability studies and the preparation of the technical file.