Readers: Reaches pharmaceutical/biopharmaceutical and medical device/instrumentation companies; academic/medical research facilities; contract research organizations, site management organizations; clinical study sites, clinical labs, drug development consulting companies, independent CRAs, and government regulatory agencies.
Focus: Hands-on articles that apply to the day-to-day activities of clinical trails, such as developing protocols, recruiting and working with human subjects, collecting and managing data, complying with the US FDA and European regulations, and addressing GCP (good clinical practice) issues. |
