Test of bacterial endotoxin, microbial limit, sterility and bacteriostatic efficacy of medical devices.

Test of ethylene oxide residues, chlorides and reducing substances in medical devices

The manufacturers of none-diaposable  medical devices that need to be sterilized, should provide at least one confirmed sterilization method, the process of which will be validated (sterilization validation).

Material characterization, reveal and determine the structural characteristics of materials by physical and chemical methods

Leachables generally refer to the substances released from medical devices or materials during clinical use, including sterilization residues, process residues,degradation products, monomers and additives (antioxidants, stabilizers, plasticizers). 

Scientific research in a laboratory with animals for acquirement of new knowledge about biology, medicine, or solving specific problems before clinical experiment.