Biovalda, Inc., with its highly qualified and experienced team offers professional solutions to public institutions and companies, universities and private enterprise for various tests and analyses required in the field of Medical Devices and Biomaterials.
Biovalda, Inc. provides various analysis and testing services required for the ISO 10993 in-vitro biocompatibility standardisations, including tests of cytotoxicity (10993-5) and blood compatibility (10993-4) which are essential for establishing standards of the medical devices and biomaterials.
Biovalda, Inc. presents sterility testing services for materials and end-products of the medical devices and pharmaceutical industry in line with the requirements of standards (ISO 11737; Ph. Eur. 7th Edition 2.6.1; USP 34 NF30 <71>)
Biovalda, Inc. offers bacterial endotoxin testing (Gel-Clot) for materials and end-products (Ph. Eur. 7th Edition 2.6.1; USP 34 NF30 <85>) within the framework of the quality requirements of the medical devices and pharmaceutical industries.
Environmental Monitoring Testing
Biovalda, Inc. provides microbial and physical monitoring testing services for the ISO 14644 and ISO 14698 Clean Room Systems in line with the quality requirements of the medical devices and pharmaceutical industries.
In-Vitro Cell Culture
Biovalda, Inc. performs testing and analysis services in a number of areas geared towards meeting the needs of universities and relevant industries, among which are introduction to basic cell culture techniques, primary cell expansion, explant cultures, cell production, and stem cells.
Biovalda, Inc.’s testing services include mechanical testings of materials and end-products of the medical devices and pharmaceutical industries, in accordance with the requirements of the quality standards.