Good Clinical Practice (GCP) eRegs & Guides - For Your Reference Book 2

Multiple Regulations at your hands on your electronic reader: 

E6 Good Clinical Practice (GCP)

Guidance for Industry Part 11, Electronic Records; Electronic Signatures — Scope and Application 

CFR 21-- General Part 11, Electronic Records; Electronic Signatures 

21 CFR PART 50 Protection Of Human Subjects 

21 CFR Part 54 Financial Disclosure By Clinical Investigators 

21 CFR PART 56 Institutional Review Boards 

Title 21 PART 312 Investigational New Drug Application 

ICH E2A Clinical Safety Data Management: Definitions and Standards for Expedited Reporting 

ICH E8 General Considerations For Clinical Trials