
Description
Founded in 1990, Fareva has grown into a global powerhouse with a presence in 12 countries and more than 40 manufacturing sites. The company specialises in delivering high-quality solutions across the entire product lifecycle, from development to commercial production. Its pharmaceutical division is renowned for expertise in sterile and non-sterile formulations, active pharmaceutical ingredients (APIs), and advanced manufacturing technologies. With a strong focus on innovation, regulatory compliance, and sustainability, Fareva partners with clients worldwide to bring their products to market efficiently and reliably.
Key Products and Services
- Pharmaceutical Manufacturing: Sterile and non-sterile production, including tablets, capsules, ointments, and injectable drugs.
- Active Pharmaceutical Ingredients (APIs): Comprehensive API manufacturing capabilities, adhering to strict regulatory standards.
- Development Services: Formulation development, process optimisation, and analytical support to ensure robust product performance.
- Packaging Solutions: Customisable primary and secondary packaging to meet diverse market needs.
- Specialised Technologies: Expertise in advanced manufacturing techniques, including lyophilisation and high-potency drug production.
Fareva's dedication to excellence and customer-centric approach has cemented its reputation as a trusted partner for pharmaceutical companies globally. By combining cutting-edge technology, stringent quality assurance, and a commitment to sustainability, Fareva continues to drive innovation and deliver value across the pharmaceutical manufacturing landscape.
Manufacturing Information
Capabilities
- Aerosol
- Ampule
- Analytical Services
- APIs (Active Pharmaceutical Ingredients)
- Asceptic Fill-Finish
- Biologics
- Blister
- Capsule
- Chemistry (CMC)
- Clean in Place / Sterilization in Place (CIP/SIP)
- Clinical Dose
- Clinical Packaging
- Clinical Trial Materials
- Containment
- Contract Development
- Contract Development and Manufacturing (CDMO)
- Contract Packaging
- Controlled Substances
- Creams & Ointments
- Cytotoxic & High Potency Compounds
- Dosage Form Development
- Dose Form
- Drug Delivery Devices
- Drug Development
- Ethical
- Filling
- Fluid Bed Processing
- Formulation Development
- Gels
- Generics
- Granulation
- High Containment Operations
- High Potency
- ICH
- Injectables
- Liquids
- Lyophilization
- Micronization
- Non Sterile Dosage
- Ophthalmics
- Oral Drug Delivery
- OTC
- Packaging
- Packaging Equipment
- Parenterals
- Powders
- Process Analytical Technology (PAT)
- Process Development
- Protein and Peptide
- Regulatory Services
- Samples
- Scale-Up
- Semisolids
- Solid Dosage
- Solutions & Suspensions
- Stability Studies
- Sterile
- Sterile Filling
- Sustained Release
- Syringe
- Tablets
- Topicals
- Unit Dosage
- Vaccines
- Vials
Contact Information
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