Contract Manufacturing
PharmaPath specializes in the out-licensing and supply of high-quality generic pharmaceutical products.
Our portfolio contains solid dosage form products suitable for Day 1 launch upon patent expiry.
We offer flexible supply chains and fully integrated services covering all stages of the pharmaceutical value chain:
Clinical Design and execution
RA support
from Regulatory Approvals to product Life Cycle Management
Manufacturing
Supply Chain Management
Our EU GMP certified production facility located in Athens, Greece, has a fully installed Operational Excellence System ensuring effective cost control and high customer service level and offers a wide variety of technologies:
Production
- Dry mixing
- Wet granulation (conventional and EX rated, High Shear Mixers and Fluid
- Bed Processors for Spray Granulation or Particles Coating)
- Drying (Tray drying, FBDs)
- Compressing (conventional, chewable, OD tablets)
- Coating (conventional or functional film coating using EX rated equipment)
- Encapsulation (hard gelatin capsules)
Packaging
- Blister packaging (conventional push through plain or perforated blisters, peel-off blisters or blisters with centered artworks using a wide variety of packaging materials)
- Secondary packaging (conventional, cartons, wide variety of leaflet sizes, booklets)
- Serialisation and Aggregation
QC testing and Batch Release to EU and International markets
Our highly skilled PharmTech team has wide experience in analytical and formulation technology transfer and plays a major role in the success of our contract-manufacturing activities. A systematic approach is followed in order to assure that the experience gained during our partner’s drug product development or commercialization is successfully transferred into commercial manufacturing to our site.
Each product eligible for contract manufacturing is thoroughly evaluated in terms of analytical methods, production process and packaging requirements. We identify and efficiently mitigate any risks prior to the introduction of a new product to our manufacturing and packaging lines, ensuring a robust and smooth technology transfer process.
Stability testing in different Climatic Zones
PharmaPath’s Quality Control Laboratory is fully equipped to support all physicochemical and microbiological tests required for the control and release of raw materials, packaging materials and finished products.
Our highly experienced QA team ensures that every production batch is manufactured, controlled and released under strict Quality and Safety standards and meets national requirements in different markets worldwide. PharmaPath has been successfully audited by the Greek National Agency and Foreign Authorities (ANVISA – Brazil, Gulf Cooperation Council – GCC, Ministry of Health of Russian Federation) as well as by an impressive number of our partners.
If you are interested in exploring a partnership for contract manufacturing with PharmaPath, please contact us at BD@pharmapath.eu
