C.O.C. Farmaceutici

About C.O.C. Farmaceutici

We are an all-Italian pharmaceutical CDMO founded around content, the constant focal point of everything we do:
liquid (such as solutions, suspensions and microemulsions), gel and lyophilized pharmaceuticals, medical devices and cosmetics, both for human and veterinary uses and especially for ophthalmic but also for nasal, oral, respiratory, otological, dermatological and diagnostic sectors. 
With decades of experience in the ophthalmic and respiratory sectors, we boast 2 companies: C.O.C. Farmaceutici and Tubilux Pharma.

Our client...

  • IT
  • 2015
    On CPHI since
  • 4
  • 250 - 499
Company types
Contact info
Meet us at

CPHI Milan 2024

Fiera Milano, Italy
08 Oct 2024 - 10 Oct 2024

Products from C.O.C. Farmaceutici (4)

  • Contract Development and Manufacturing

    Product Contract Development and Manufacturing

    We are a Pharmaceutical contract development and manufacturing company authorised for the preparation of medicinal products and medical devices in liquid, suspension, gel and cream form, lyophilisates and ointments. Our services include formula development, pilot studies in the laborato...
  • Products in Private Label

    Product Products in Private Label

    We offer customers a complete range of medical devices for nasal and eye care, ready for customisation with the graphics and brand of the distributor. They are CE-marked and can be sold in EU and non-EU countries, once they have been registered locally.
  • R&D and Industrialization

    Product R&D and Industrialization

    We specialise in research and development in the ophthalmic field for multinationals, Italian as well as international pharmaceutical companies. For them, we develop, fine-tune and manufacture, in aseptic conditions, pharmaceuticals and sterile medical devices for topical use in differen...
  • Regulatory services

    Product Regulatory services

    For pharmaceutical products, we offer support for regulatory services such as:
    registration via national and European Union procedures;ANDA registration;
    drafting of e-CTDs to create e-CTD sequences;
    regulatory compliance;
    minor and major variations (evaluation and/or management).For ...