Toxicology / Biocompatibility
Biocompatibility is the process of evaluating materials used in the manufacture of medical devices. It consists of a number of tests designed to provide assurance that the final product, when used as indicated, will be safe. While some materials have been tested, other materials and chemical components have not. Read More.
An important part of the manufacturing process for medical devices is determining the level and nature of viable microorganisms that are generated as a result of the process. By developing and following a routine, documented sampling plan, you are assured that your process remains under control. Read More.
Geneva Laboratories’ chemistry department provides quality compendial and non-compendial chemical analysis of raw materials and final product. Compendial testing of pharmaceuticals (APIs and drug products), food additives, and reagent chemicals is performed under many compendia. Read More.
Geneva Laboratories offers a wide range of storage conditions including “extreme low temperature,” refrigeration, and elevated humidity. By applying ICH/FDA and ASTM (Q10) guidance, our analysts will work with you to set up protocols using the best temperature and humidity conditions for your product. Read More.