Analytical Equipment - R&D Process Equipment - Tablet Presses - Capsule Fillers - Liquid and Powder Filling Lines - Blister Packing - Cartoning - Labelling - End of Line Packaging - Compression Tooling - Change Parts

cGMP Reconditioned Equipment

We comply with pharmaceutical industry’s current Good Manufacturing Practice (cGMP). We have developed a cGMP reconditioning programme that effectively upgrades used production equipment, which has proved particularly popular with tablet compression and processing equipment as it offers significant savings against new machinery.

All equipment reconditioning and/or modification can be carried out to individual customer specifications under the supervision of our own highly trained and experienced engineers. From new CE marked control panels to re-calibration, all components and equipment are fully tested and factory acceptance trials are conducted with customers prior to dispatch. In addition (for validation purposes) we offer component calibration certification and IQ & OQ validation documentation.

Furthermore, to maintain the machine integrity, we try to use parts from the original component manufacturer, thus making re-validation that much easier.