Research & Development.
The EVER Group attaches particular importance to research and development. Through our in-house R&D expertise, we bring specialized therapeutic solutions to market that support healthcare systems around the world.
Our goal is to provide physicians with the optimal preparation and therapy concept to ensure the best possible treatment for patients.
EVER Pharma has more than 30 years of experience and know-how in the field of neuroscientific research with a clear focus on neurodegenerative and cerebrovascular diseases. Our own research facilities and collaborations with international research institutes ensure the successful further development of our product portfolio.
Our R&D capabilities are focuesd on five areas:
- Preclinical research
- Pharmaceutical development
- Medical device development
- Clinical development
- Regulatory affairs
EVER Pharma combines experience from over 60 years of sterile production with innovative know-how and high-quality manufacturing technology. Our GMP-compliant production facility in Jena, Germany, produces more than 400 different finished medicinal products.
We manufacture and pack high-quality complex injectables including high potency and controlled substances, crystal suspensions, as well as oily solutions in vials, pre-filled syringes, cartridges, implants, and ampoules are produced for the supply of EVER Pharma’s products around the world as well as third party customers.
Our facilities can handle sterile hormone synthesis in suspension, oily solutions, cytotoxics, and controlled substances.
All products are manufactured under clean room conditions according to EU-GMP guidelines or country-specific quality requirements. EVER Pharma is certified according to EU GMP requirements as well as ISO 13485, ISO 16247, ISO 14001, EU-GMP, GCC (MENA), CFDA (China), ANVISA (Brazil), RU-GMP, and PDMA (Japan).
We are specialized in the manufacture of complex, injectable substances with a special focus on:
- Handling of highly active substances (e.g. narcotics, hormones, cytotoxics)
- Low-oxygen formulations
- Crystal suspensions
- Oily solutions
We also offer our customers support for development, regulation, production, and testing:
- Validation, analytical services, and clinical batch manufacturing
- Commercial manufacture of sterile dosage forms
- Secondary packaging and storage
- Optimization of formulations and processes
- Analytical testing of sterile dosage forms
- Stability test
- Technical advice
|Production capacities||Up to 130 million units / year|
|Pre-filled syringes||Pre-filled syringe sizes: 1, 2, 3 and 5 ml (glass or plastic)|
|Vials||Vial sizes: 2, 5, 10, 20 and 50 ml|
|Ampoule||Ampoule sizes: 1, 2, 3, 5, 10, 12, 15, 20 and 25 ml|
|Inspection||Automatic inspection lines for ampoules|
Semi-automatic and manual visual inspection of vials and pre-filled syringes
|Packaging||Automtaic packaging lines |
Semi-automatic packaging line for vials and pre-filled syringes
|Storage capacities||Up to 5,500 pallets|
|Number of employees||Approx. 400|
|Official certifications||ISO 13485, ISO 16247, ISO 14001, EU-GMP, GCC (MENA), CFDA (China), ANVISA (Brazil), RU-GMP, PDMA (Japan)|
EVER Pharma has a global marketing reach and sells its products in over 70 countries worldwide. Our international network of over 25 wholly owned affiliates, together with our strategic partners, provides both a broad geographical footprint and local marketing expertise.
This enables EVER Pharma to locally support patients and customers and react quickly to the changing dynamics of individual markets.