Description
NextPharma are a leading Pharmaceutical and Nutraceutical CDMO with 10 manufacturing sites in Europe. Each site is able to develop and produce dosage forms from the pre-clinical stage, through to commercialisation and routine supply.
Our expertise covers a wide variety of solid oral dosage forms, alongside liquids, suppositories, topical and ophthalmic products. Each site acts as a centre of excellence for at least one of these technologies.
Our NextPharma teams are vastly experienced in overcoming developmental challenges such as:
- Poor Aqueous Solubility
- Reduced Bioavailability
- Highly Potent APIs
- Sustained/Controlled Release Profiles
- Controlled Drug Substance
Type of Drugs Manufactured:
Small Molecule
CDMO Services:
Drug Product Formulation (FDF);Research & Development;Clinical Trials materials and logistics;Packaging;Regulatory Services;Analytical Development
No. of Manufacturing Facilities:
6-10
Please select any High Potent Products capabilities:
OEB 3;OEB 4-5;OEB >5
Facilities Locations:
Europe
Regulatory Approvals for your facilities:
FDA (United States);EMA (Europe);ISO;GMP;ANVISA (Brazil)
Manufacturing Technologies:
Blow-Fill-Seal (BFS);Liquids;Lyophilized amps/vials;Semi-solids;Soft Gels;Solids
Current Capacity:
Drug Product Formulation (FDF);Research & Development;Clinical Trials materials and logistics;Packaging;Regulatory Services;Analytical Development
NextPharma continues to enhance its offerings to meet the evolving needs of the pharmaceutical industry. For more information, please visit nextpharma.com.
Capabilities
- Analytical Methods Development
- Analytical Services
- Biologics
- Clinical Dose
- Clinical Packaging
- Clinical Trial Materials
- Containment
- Contract Development and Manufacturing (CDMO)
- Drug Product Formulation (FDF)
- Finished Dosage Forms
- Non Sterile Dosage
- Packaging
- Regulatory Services
- Research & Development
- Small Molecule
- Solid Dosage
Contact Information
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