Thursday, December 3, 2015

Seminar on Equipment, Facility, and Process Qualification and Validation - A Simple Top to Bottom Sustainable Approach - St. Petersburg, FL

December 3, 2015 at 9am to December 4, 2015 at 6pm – Courtyard St. Petersburg Downtown,300 4th St N, St Petersburg, FL 33701, United States Course "Equipment, Facility, and Process Qualification and Validation - A Simple Top to Bottom Sustainable Approach" has been pre-approved by RAPS as eligible for up to 12 credits towards a participa… Organized by NetZealous LLC - DBA GlobalCompliancePanel | Type: seminar
2-day In-person Seminar on Validation and Part 11 Compliance of Computer Systems and Data at Mumbai, India

December 3, 2015 at 9am to December 4, 2015 at 6pm – The LaLiT Mumbai Overview: Analytical equipment should be qualified and computer systems should be validated to demonstrate suitability for the intended use. Electronic records must comply with FDA Part 11 and EU/PIC… Organized by John Robinson | Type: conference
Seminar on Cyber Security Incident Response Program (CSIRT) and Plans - at San Francisco, CA

December 3, 2015 at 9am to December 4, 2015 at 6pm – DoubleTree by Hilton Hotel San Francisco Airport , 835 Airport Blvd., Burlingame CA 94010-9949 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 NetZealous LLC, DBA GlobalCompliancePanel | Type: seminar
Seminar on Safe Production of Meat Products - at St. Louis, Missouri

December 3, 2015 at 9am to December 4, 2015 at 6pm – Courtyard St Louis Downtown, 2340 Market St, St. Louis, Missouri 63103, United States 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 NetZealous LLC - DBA GlobalCompliancePanel | Type: seminar
Webinar on Medical Device Tracking: Latest FDA Update and Expectations

December 3, 2015 from 10am to 11am – Online Overview: The Food and Drug Administration Modernization Act (FDAMA) requires that manufacturers track certain devices when the agency orders them to do so.Tracking is intended to facilitate notifica… Organized by Adam Fleming | Type: webinar
Webinar on Serious Adverse Events (SAEs): What it is and How to Handle

December 3, 2015 from 10am to 11am – Online Event Overview: When conducting clinical trials it is important to understand and be able to identify serious adverse events(SAE). These are events that are serious, likely related to the study drug, devic… Organized by Netzealous -MentorHealth | Type: online, healthcare, training, courses
Webinar On Metrology: Statistical Analysis of Measurement Uncertainty

December 3, 2015 from 1pm to 2:30pm – Online Description : The seminar begins with an examination of the fundamental vocabulary and concepts related to metrology. Topics include: accuracy, precision, calibration, and "uncertainty ratios". Sever… Organized by compliancetrainings | Type: webinar
Webinar On FDA vs EU Inspections – Differences and How to Get Prepared

December 3, 2015 from 1pm to 2pm – Online Description : This training is a comparative look at FDA & EU regulations to help attendees understand the FDA and EU inspection process and how to prepare for both of them. Attendees will learn… Organized by Compliance Trainings | Type: webinar
Webinar On Medical Device Laws and Regulations in Asia: China, Hong Kong, Japan and Korea

December 3, 2015 from 1pm to 2pm – Online Description : This webinar is intended to help you get familiar with medical device laws and regulations in Asian countries: China, Hong Kong, Japan, and Korea. The medical devices are currently one… Organized by Compliance Trainings | Type: webinar