About us

 

KATO Labs was established in 1994 as a Pharmaceutical Company operating on the Polish market. KATO Labs cooperates with all pharmaceutical distributors. We have our own unique products. KATO Clinical has been operating on the clinical trial front since 2005. We have high tech facilities in Warsaw and Slupsk to store materials for clinical trials. We fulfill all European Union standards.

Kato Clinical offers a variety of services that you need to expedite the start, execution and completion of your Clinical Trial.

Kato Clinical adheres to all GCP and GMP Regulations affecting the Manufacture, Packaging, Labeling, Release, Storage, Distribution, Return, Accountability, and Destruction of Clinical Trial Materials.

Kato Clinical can arrange for the manufacture, blinding, packaging, labeling, analytical, and release (both Q.P. Technical and Q.P. Regulatory Green Light) in the USA and Japan for immediate import and use in the E.U.

Get an offer

 

Documents

KATO Clinical Certificate of GMP

Download (PL)
Download (EN)

KATO Clinical Manufacturer License

Download (PL)
Download (EN)

KATO Clinical Import License

Download (PL)
Download (EN)

KATO Clinical Trial Relabeling Permit

Download (PL)
Download (EN)

KATO Clinical Trial Psychotropic Permit

Download (PL)
Download (EN)

Copyright © 2017. All rights reserved.
Phone: +48 22 816 1450