Friday, December 11, 2015

Seminar on Validation and Part 11 Compliance of Computer Systems and Data at Sydney, Australia

December 10, 2015 at 9am to December 11, 2015 at 6pm – Hilton Sydney, 488 George Street, Sydney, Australia 2000 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 NetZealous LLC, DBA GlobalCompliancePanel | Type: seminar
Seminar on Modern Approaches to Process Validation: Requirements for Process Design, Design of Facilities and the Qualification of Equipment and Utilities at Copenhagen, Denmark

December 10, 2015 at 9am to December 11, 2015 at 6pm – Copenhagen, Denmark Overview:Companies face many common issues and confusion when creating or revamping their validation programs. Some of these common issues are:• Company has expertise in its process validation progra… Organized by NetZealous LLC, DBA GlobalCompliancePanel | Type: seminar
Seminar on Mastering Biofilm Control, Monitoring, Validation and Excursion Investigations of Pharmaceutical Water Systems at Boston, MA

December 10, 2015 at 9am to December 11, 2015 at 6pm – Boston, Massachusetts Course "Mastering Biofilm Control, Monitoring, Validation and Excursion Investigations of Pharmaceutical Water Systems" has been pre-approved by RAPS as eligible for up to 12 credits towards a partic… Organized by NetZealous LLC - DBA GlobalCompliancePanel | Type: seminar
Webinar: Vaccine Studies – Operationalize before you Finalize

December 11, 2015 from 11am to 12pm – Online This webinar will explore the following areas of early preparation in vaccine studies: Important operational questions to ask before finalizing the protocol Incorporating feedback from an experience… Organized by Xtalks Life Science Webinars | Type: webinar, (free)
Webinar on Risk Assessment for Medical Devices

December 11, 2015 from 1pm to 2pm – Online Description : The secret to preventing medical device recalls or at least to minimizing their impact is sound Risk/Hazard Analysis. Aside from being required, it is absolutely essential and necessary… Organized by Compliance Trainings | Type: webinar
Webinar: FDA Expectations for 503B Outsourcing Facilities

December 11, 2015 from 1pm to 2pm – Online Are you a compounding pharmacy considering whether to register with the FDA as an Outsourcing Facility? Are you already an outsourcing pharmacy wondering why so many 503B facilities are receiving FDA… Organized by Xtalks Life Science Webinars | Type: webinar, (free)