Pharmaceutical Industry CGMP guidelines are an integral part of Kinematica compliance with the highest of the world’s regulatory standards. Complete safety to ensure low-risk product manufacturing in sterile environments as well, is part of Kinematica’s long-lasting experience in supplying specialized solutions to the largest pharmaceutical companies around the world. Comprehensive expertise for seamless integration with quality control and other specialized clean-room systems can also be offered.
BENEFITS: EXECUTIVE OVERVIEW
- Highest results reproducibility for an extremely narrow particle size distribution in accordance to the most demanding specifications
- Fully controlled homogenizing with industry-leading shear rates of up to 300 000 s-1
- Full CIP / SIP compliance and comprehensive certification in accordance to the widest acknowledged standards by including highest class clean-room for complete sterile environments and zero-contamination
Aseptic formulation of pharmaceuticals
Adjuvant for vaccines
Chicken embryos for yellow fever vaccine