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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.


Standard Operating Procedures for Good Clinical Practice by Sponsors of Clinical Trials
Standard Operating Procedures for Good Clinical Practice by Sponsors of Clinical Trials
Electronic onlyPrice: $3,900.00 
Standard Operating Procedures for the Conduct of Clinical Research
Standard Operating Procedures for the Conduct of Clinical Research
Electronic onlyPrice: $595.00 
Policies and Standard Operating Procedures for the Institutional Review Board, Third Edition
Policies and Standard Operating Procedures for the Institutional Review Board, Third Edition
Binder/CD-ROMPrice: $1,750.00 
Standard Operating Procedures for Good Clinical Practice by Sponsors of Medical Device Clinical Trial
Standard Operating Procedures for Good Clinical Practice by Sponsors of Medical Device Clinical Trial
Binder/CD-ROMPrice: $4,200.00