Content Group | Sant´Agata Bolognese

Content Group | Sant´Agata Bolognese

COC Farmaceutici srl: registered office; manufacturing facility

About the plant

Content Group is an all-Italian pharmaceutical CDMO composed of COC Farmaceutici and Tubilux Pharma. The Group develops and manufactures liquid, gel, cream and lyophilized pharmaceuticals, medical devices and cosmetics for human and veterinary use. With decades of experience in ophthalmic and respiratory sectors, Content Group is among Europe’s leading players, serving partners worldwide with full CDMO services, innovation and quality as core values.

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COC Farmaceutici | Sant’Agata Bolognese (BO)

The Sant’Agata Bolognese site serves as the registered office of COC Farmaceutici and operates as a manufacturing facility for liquid and gel formulations dedicated to pharmaceuticals (human and veterinary) and sterile class A medical devices.

Certifications:
ISO 13485 – Manufacturing of Medical Devices
GMP Plant – Approved by AIFA for aseptically prepared sterile liquid drugs (human) and by the Italian Ministry of Health for veterinary drugs

2024 Production Volumes:
• 4,4 million bottles
• 19,5 million strips of 5 plastic ampoules

Main Sectors:
Ophthalmic | Respiratory | Veterinary

Primary Packaging Formats:
Strips of 5 plastic ampoules | Multidose bottles | Preservative-free bottles

 

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Certifications

• ISO
• EMA (EU GMP)

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Activity

• Inhalation products, Sterile forms (ophtalmic, nasal, otic), Aerosol, Nebulization, Fill&Finish, Bottles, Ophtalmic dispensers, FDF / DRUG PRODUCTS, SERVICES manufacturing

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Features

• Uses: Commercial (Phase IV), Human, Veterinary
• Toxicity (OEB classification): N/A
• DEA: N/A
• BSL: N/A
• Therapeutic areas: (R) Respiratory system, (S) Sensory organs
• Markets: EMA (EU)

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Batch Size / Reactor

• Medium, Large

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Services

• Regulatory services, Development services, Manufacturing services, Analytical / QC services, Quality Assurance services, Packaging, Logistics, Preformulation studies, R&D, Formulation / Galenic design, Process development, Process optimization, Process validation, Stability studies design, Stability studies execution, Tech transfer, Pilot plant, Formulation mixing, Scale-up, Pilot batches, Batch records, Analytical methods development, Analytical methods validation, Analytical methods transfer, QP in house, Primary packaging, Secondary packaging, Labeling, Storage, CTD/eCTD compilation and submission

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