Thursday, April 16, 2015

Why is FDA at my Facility, and What do I do During an Inspection - GlobalCompliancePanel

April 16, 2015 at 9am to April 17, 2015 at 6pm – Hong Kong Overview: Many regulated companies preparing for FDA inspections are not prepared and the outcome can be negative as we see all the time with enforcement actions. This seminar provides the fundamenta… Organized by GlobalCOmpliancePanel | Type: food, fda, medical, device, defence, and, navy, aerospace, mining
Safe Production of Meat Products - In-person Comprehensive Workshop

April 16, 2015 at 9am to April 17, 2015 at 6pm – Courtyard St Louis Downtown Overview: Educational material discussed during this seminar will include both effective sanitation and hygienic practices and the control of microorganisms that cause spoilage and foodborne illness.… Organized by GlobalCompliancePanel | Type: food, fda, medical, device, aerospace, navy, and, defence
Cyber Security Incident Response Program (CSIRT) and Plans - 2-day In-person Workshop

April 16, 2015 at 9am to April 17, 2015 at 6pm – Baltimore, MD Overview: Cyber Security Incident Response Program is a must for any organization using the Internet. It must be robust yet flexible. Unfortunately in spite of all of the Cyber Events, many companies… Organized by GlobalCOmpliancePanel | Type: food, fda, medical, device, defence, and, navy, aerospace, mining
Webinar On FDA Regulation of Mobile Apps

April 16, 2015 from 1pm to 2pm – Online Description: The use of mobile apps as a medical device continues to mushroom. Approximately 85% of adults use cell phones. They offer a fertile field for mobile apps used for medical purposes, some… Organized by Compliance Trainings | Type: webinar
Webinar On 21 CFR Part 820 - Quality System Regulation - Applying Principles of Lean Documents and Lean Configuration

April 16, 2015 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 o… Organized by Compliance Trainings | Type: webinar
Webinar On Current Good Manufacturing Practices (cGMP) for Medical Devices and IVDs

April 16, 2015 from 1pm to 2pm – Canada Description : The US Food and Drug Administration (FDA) states in warning letters “this inspection revealed that these devices are adulterated within the meaning of section 510(h) of the FD&C Act… Organized by Compliance Trainings | Type: webinar
Webinar On Transfer of Analytical Methods and Procedures according to USP 1224

April 16, 2015 from 6pm to 7pm – Online Description : When validated methods are transferred between laboratories and sites, their validated state should be maintained to ensure the same reliable results in the receiving laboratory. For a… Organized by Compliance Trainings | Type: webinar