Description
INCOG BioPharma Services is a contract development and manufacturing organisation (CDMO) dedicated to delivering superior solutions for the global injectable drug product market.
With world-class facilities and state-of-the-art equipment, INCOG BioPharma Services offers comprehensive support from development to commercialisation of injectable drug products. The company prides itself on its consultative approach, ensuring that each client receives tailored solutions that prioritise patient safety and product efficacy. By integrating decades of industry experience, INCOG has established processes designed to enhance and accelerate the delivery of life-saving medicines to market.
Key Products and Services:
Drug Product Development: Expertise in formulating and developing injectable therapies to meet specific client requirements.
Aseptic Fill-Finish Manufacturing: State-of-the-art facilities for sterile filling of vials, syringes, and cartridges.
Analytical and Quality Control Testing: Comprehensive testing services to ensure product integrity and compliance with regulatory standards.
Packaging and Labelling: Customised packaging solutions designed to maintain product stability and facilitate patient use.
Regulatory Support: Assistance with navigating complex regulatory pathways to expedite product approval and market entry.
INCOG BioPharma Services is committed to redefining the CDMO experience by acting as an extension of the clients it serves. Every decision is made with the patients' best interests in mind, ensuring better outcomes delivered on time and within budget.
Manufacturing Information
Capabilities
- Accelerated Stability Studies
- Analytical Services
- APIs (Active Pharmaceutical Ingredients)
- Asceptic Fill-Finish
- Bioanalytical Services
- Biologics
- Bioprocessing
- Biosimilars
- Cartridge
- Chemistry (CMC)
- Clean in Place / Sterilization in Place (CIP/SIP)
- Clinical Dose
- Clinical Packaging
- Clinical Trial Materials
- Clinical Trials
- Cold Chain Management
- Contract Development and Manufacturing (CDMO)
- Disposable/Single-Use
- Documentation Support Services
- Dose Form
- Feasibility Studies
- Filling
- Finished Dosage Forms
- Formulation Development
- Generics
- Glass
- ICH
- Injectables
- Labelling
- Large Volume
- Liquids
- Oligonucleotides
- Ophthalmics
- Packaging
- Parenterals
- Peptides
- Preclinical Testing
- Process Development
- Process Validation Studies
- Project Management
- Proteins
- Quality QA/QC
- Regulatory Services
- Safety & Environment (HS&E)
- Scale-Up
- Solid Dosage
- Solutions & Suspensions
- Stability Studies
- Sterile
- Sterile Filling
- Sterility Testing
- Sterilization
- Storage
- Syringe
- Technology Transfer
- Vaccines
- Validation
- Vials
- Warehousing
Contact Information
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