SOPs for Clinical Research
Standard Operating Procedures (SOPs) are critical to an organization’s quality
performance and the ethical conduct of clinical trials while helping to create and sustain
a successful clinical trial program. CenterWatch has made developing these procedures easy
with four customizable templates for sponsors, IRBs and investigative sites to aid in
documenting policies that reflect your company’s philosophies, standards and
innovations while complying with federal regulations and requirements. Each binder includes
a CD-ROM (optional for Site SOP), forms, checklists and study management materials.