Clinical Master Reference Guide 210 Each attendee will be logged

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

International GMP Master Guide

Annex 19 - Reference and Retention Samples

A GMP Publications representative will contact the purchaser for the email address(es) of each attendee who purchases a Desk Reference Set

Master GMP Trainer - US FDA Title 21 CFR Parts:

Clinical Master Reference Guide 210 Each attendee will be loggedThe 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