6-Hour Virtual Seminar on Auditing Analytical Laboratories for FDA Compliance

If you are unable to see the message below, [click here to view](. [Logo]( 6-Hour Virtual Seminar [6-Hour Virtual Seminar on Auditing Analytical Laboratories for FDA Compliance]( [REGISTER NOW]( It is critical that the audit of the laboratory be conducted in a professional manner, as a poor audit will waste money and lead to a false confidence in the abilities of the audited laboratory whether it is internal or external to the company. Date: Tuesday, January 14, 2020 Time: 08:00 AM PST | 11:00 AM EST Duration: 6 Hours Instructor: Steven S Kuwahara Overview: There are two phases to this topic. The first is auditing itself. Good audits are well structured. They must consider the reasons for the audit, the regulatory requirements, as well as the nature of the laboratory being audited. We will discuss the considerations that must be made when auditing a laboratory. The social interactions that must be expected, the nature of the regulatory requirements and the nature of work that the laboratory performs will be discussed.[Read more..](. Who Will Benefit: - Potential Auditors - Supervisors who must initiate Audits - Laboratory Supervisors and Workers - Quality Assurance and Control Supervisors and Lead Workers - Supervisory Management who must select Contractors - Managers - Directors - Vice Presidents who Supervise Quality Assurance - Quality Control - Regulatory Affairs Groups About Speaker: Joy McElroy Principle Consultant, Maynard Consulting Company Dr. Joy McElroy, Upon earning a degree in Zoology at North Carolina State University, Joy made her debut in the pharmaceutical industry in 1992 at Pharmacia & UpJohn performing Environmental Monitoring and Sterility Testing. [Read More]( GlobalCompliancePanel 39658 Mission Boulevard, Fremont, CA 94539, USA. Toll Free: +1-800-447-9407 Fax: 302 288 6884 [www.globalcompliancepanel.com]( | [Unsubscribe]( Copyright © 2019 GlobalCompliancePanel. All rights reserved.