Hosmotic company
Hosmoticsrl comes from the experience in the field of advanced analytical techniques regarding food processing, pharmaceuticals, biotechnology and industrial.
Soon the company specializes its expertise in the field of analytic applications applied to process control of supercritical CO2-based systems of high technology, with the purpose of research & development, as well as applied to modern industrial production processes. The degree of innovation and constant updating are also favored by many academic contacts and collaborations with many organizations in the field of technology.
Processes:
- SFE extraction
- SFF fractionation
- SFP pasteurization Micronisation
- SFM Chromatography Purification
- SFC Extraction with H2O high pressure SFWE
The rapid integration of this modern technology with advanced spectrometric or chromatographic analytical systems generally completes the technological structure at the base of the system, optimizing applications and making the production cycles most competitive
The high specialization of a highly qualified team launches Hosmotic towards the current multisectorial profile, in which it operates throughout the chain of analytical chemistry and chemical engineering, at both laboratory and industrial level.
The great technical and scientific expertise, the constant control of all operational procedures and the relentless pursuit of the highest level of technology and professional, configures Hosmoticsrl as an ideal partner in industry and scientific research.
The long experience in this field allows a great ability to listen, to understand in depth the expectations of each client and plan interventions based on which the real needs are.
Method validation has received considerable attention in the literature and from industrial committees and regulatory agencies. The U.S. FDA CGMP request in section 211.165 (e) methods to be validated: The accuracy, sensitivity, specificity, and reproducibility of test methods employed by the firm shall be established and documented. Such validation and documentation may be accomplished in accordance with Sec. 211.194(a). These requirements include a statement of each method used in testing the sample to meet proper standards of accuracy and reliability, as applied to the tested product. The U.S. FDA has also proposed industry guidance for Analytical Procedures and Methods Validation.