ANALYST REPORT - The CDRH (Center for Devices and Radiological Health) is in the process of updating their standards and suggested practices. They are going to be more strict with medical device developers. The purpose of this paper is to present the medical device developer guidelines for complying with the "suggestions" of the CDRH.
Posted: May 13, 2009 | Published: March 31, 2009


Topics:  FDA | FDA Compliance | Medical Software | Software | Software Project Management | Software Quality Assurance | Standards

WHITE PAPER - Our Healthcare Industry page is the place to start if you need to stay up-to-date on related subject areas, such as Medical Hardware and Software, Telemedicine, and Biotechnology.
Posted: February 13, 2006 | Published: February 13, 2006


Topics:  FDA | FDA Compliance | Health Care Applications Software | Health Care Industry | HIPAA | HIPAA Compliance | Medical Records Management | Pharmaceutical Industry | Telemedicine