Clinical Master Reference Guide 210 Part 50 - Protection of

Part 50 - Protection of Human Subjects

ICH E6(R3) Good Clinical Practice

Each attendee will be logged into the Webinar with their own unique email address for accountability and all Attendees must satisfy 7 hours of 'eye's on' training to get a certificate of attendance

The GMP 210/211 regulations address issues including recordkeeping

Checklist for GCP Systems Gap Analysis

Clinical Master Reference Guide 210 Part 50 - Protection ofThe 600+ page GCP Master Handbook is a complete reference library for the clinical professional. This handbook comes in a easy to carry 4. 5" x 7. 5" pocket size booklet for quick access to standards and references. Includes: US FDA Title 21 CFR Parts Part 11 Electronic Records Part 50 Protection of human subjects Part 54 Financial disclosure by clinical investigators Part 56 Institutional Review Boards Part 312 Investigational New Drug Application