Pharmaceuticals
We collaborate with pharmaceutical companies focused on the innovation and development of new products, including new formulations and compositions, pharmaceutical forms, presentations and therapies.
Pharmaceuticals
We collaborate with pharmaceutical companies focused on the innovation and development of new products, including new formulations and compositions, pharmaceutical forms, presentations and therapies. Our scope is to offer to our partners Advanced Generic Pharmaceuticals developed in-house with the potential to become the first or the second generic in selected markets. Our keen interest in research and innovation led us to develop several high-technology processes for manufacturing novel delivery systems and different products.
- PELLETS TECHNOLOGY DEVELOPMENT
- TASTE MASKING
- CEPHALOSPORIN MANUFACTURING UNIT
- ORALLY DISINTEGRATING STRIPS
Our Technology for New Innovative Products
MICRO EMULSION COATING (MECT)
heck marMicro-Emulsion Coating Technology (MECT) is used for the solubilization of oil-soluble drugs and liquids in the oil phase, followed by micro-emulsification with an aqueous phase containing a polymer to coat the substrate.
PELLET COLD FORMING (PCFT)
Pellet Cold Forming Technology (PCFT) is used for heat-sensitive materials that either lose potency or transform into another form when processed at normal temperatures.
RAPID GELATION DRUG RELEASE (RGDRT)
Rapid Gelation Drug Release Technology (RGDRT) is used to release drugs with pseudo-zero-order kinetics and serves as an alternative to OROS® technology.
MATRIX PORE FORMING (MAPOTAB)
Matrix Pore Forming Tablet Technology (MAPOTAB) is applied for drug release through pores into aqueous media.
Oncological Products
We are also focused on the development of innovative oncology injectable drugs, innovative ADC drugs, and other biologics. Our goal is to make innovative medicines that are affordable for patients. TOLLEON specializes in offering injectables drug development and manufacturing. We offer CDMO/CMO services for specific injections.
Formulation Development
- Drugability study
- Formulation development
- Lyophilisation process development
- Fill/finish process development
- Pre-filled syringe product development
- High concentration formulation and fill/finish process
Quality Management
Our products are developed and manufactured under strict criteria in certified pharmaceutical production units complying with EU, FDA, and WHO GMP standards, certified with EN ISO 9002 from TUV CERT Germany. Our laboratory developments are carried out at approved EU pharmaceutical laboratories under the supervision of a team of specialized chemists.