Tuesday, January 9, 2018

Pharmaceutical Validation Guidelines | 21 CFR Part 11 Compliance 2018

January 8, 2018 at 9am to January 9, 2018 at 6pm – Zurich, Switzerland Course "Validation and 21 CFR Part 11 Compliance of Computer Systems" has been pre-approved by RAPS as eligible for up to 12 credits towards a participant's RAC recertification upon full completion… Organized by NetZealous DBA as GlobalCompliancePanel | Type: regulatory, and, compliance, seminars
Ensuring Data Integrity and Safety in Clinical Research

January 9, 2018 from 10am to 11am – Fremont Overview: Electronic medical records and electronic handling of study data is increasingly common. To involve computer systems in clinical research implies knowledge of 21 CFR Part 11. Why should you… Organized by Event Manager | Type: online
Webinar On "Supplier Quality Management Utilizing Principles of Lean Documents and Lean Configuration"

January 9, 2018 from 1pm to 2:30pm – Online Description : All life science businesses are required to maintain their Quality Management System (QMS) processes in a state of control, via controlled documents and objective evidence in the form… Organized by Sam Miller | Type: online, /, webinar