For more than 20 years, TechnoSTAT has been providing pharmaceutical, medical device and biotechnology companies with cutting edge services in the areas of: • Clinical trial management and monitoring (CRO) • Data management (EDC and paper) • Biostatistics and trial design (including protocol development) • Interaction with regulatory authorities We offer services from early stage non-clinical development and bench testing, to all clinical study phases in protocol development, clinical trial management, through submissions to, and consultations with, regulatory agencies such as FDA, EMA and European certification authorities. TechnoSTAT has a long and successful track record serving clients internationally, including dozens of regulatory approvals in both U.S. and Europe. We are committed to the highest industry standards, conforming to SOPs complying with GCP and other relevant regulatory requirements. Our Company will support your product's regulatory approval, as well as aid in subsequent post-market activities. TechnoSTAT will provide your organization with all the statistical, CRO and data handling needs you have. We invite you to contact us about your upcoming or ongoing clinical programs.
