Our pharmaceutical production experience and expertise enable us to offer a comprehensive solution that includes a range of benefits designed to facilitate and optimize the integration of TRICAP and CAPELEV machines into your production line.
GMP compliances services
- Implementation and documentation of the FAT (Factory Acceptance Test).
- Realization of the IQ/OQ/PQ validation protocols.
- Certificates of materials for all parts in contact with the product.
- Instruction manual.
- Certificates of Metrology for size parts.
Additional services
- Achievement of a selection test on capsules samples to validate sorting possibilities (documented test report).
- Demonstration “in situ” on the actual conditions of production (only possible in the Europe West area).
- Simulation with 3D drawings of the different possibilities of integration.
- Installation and training of users (trilingual French, Spanish, English).
- Realization of “tailor-made” solutions to perfectly integrate our equipment into the line of production (completion of transfer ramp, special adaptations…).
- Technical assistance service (trilingual French, Spanish, English).
- Service of Metrology for dimensional monitoring of the size parts in service (annual control with documented report).