Tuesday, January 18, 2022

Verification and Validation - Product, Equipment/Process, Software and QMS

January 18, 2022 at 9am to January 19, 2022 at 4pm – online Develop / review a company's Master Validation Plan for major cGMP deficiencies. Address the U.S. FDA's newer and tougher regulatory stance. One major failing is lack of sufficient or targeted risk-b… Organized by Complianceonline | Type: seminae
Overview of the Financial Aspects of Clinical Research

January 18, 2022 from 10am to 1pm – online The financial processes supporting a clinical research study is arguably the most important aspect of the study’s life cycle. Without an understanding of clinical research finance, organizations and… Organized by Complianceonline | Type: webinar
Overview of the Financial Aspects of Clinical Research

January 18, 2022 from 10am to 1pm – online The financial processes supporting a clinical research study is arguably the most important aspect of the study’s life cycle. Without an understanding of clinical research finance, organizations and… Organized by Complianceonline | Type: webinar
IT Auditing - Principles and Practices for Executives and Directors

January 18, 2022 from 10am to 1pm – online This IT Audit webinar facilitates an executive-level understanding of the ISACA IT Auditing Standards associated with performing IT assurance services and accepted areas of risk for most organization… Organized by Complianceonline | Type: webinar
Investigation of Out-of-Specification Test Results

January 18, 2022 from 10am to 1pm – online Attendees will learn the FDA expectations when investigating out-of-specification and out-of-trend laboratory results. Why Should You Attend: Attendees will learn how to streamline and conduct timely… Organized by ComplianceOnline | Type: webinar