The Cutting Edge of Medical Technology Content, Community & Collaboration
April 23, 2019 at 9am to April 24, 2019 at 6pm – DoubleTree by Hilton Philadelphia Airport Description: This course is designed to provide a microbiology-focused education about all aspects of water systems and how biofilm manages to thrive there. Prior microbiological education or train… Organized by John Robinson | Type: seminar, on, validation, and, troubleshooting, of, pharmaceutical, water, systems
November 12, 2015 at 9am to November 13, 2015 at 6pm – Mandarin Orchard Singapore, 333 Orchard Road, Singapore 238867 Overview: This course will present the regulations and guidelines that apply to operations in quality control testing laboratories. In some cases these will not be specific regulations, but needs tha… Organized by John Robinson | Type: conference, pharmaceutical, quality, control, seminar
May 9, 2013 from 10am to 11am – Online Training Overview: Major postmarketing vigilance revisions are now in force. A revised medical device guidance document on postmarketing vigilance (MEDDEV 2.12-1 rev 5) came into force on January 1, 2008. Pro… Organized by GlobalCompliancePanel | Type: webinar, healthcare, medical, device, pharmaceutical, clinical
May 8, 2013 from 10am to 11am – Online Training Overview: Understanding, interpreting, and implementing design control requirements in a holistic manner can significantly expedite the regulatory processes, bringing innovative medical products to t… Organized by GlobalCompliancePanel | Type: webinar, healthcare, medical, device, pharmaceutical, clinical
May 8, 2013 from 10am to 11am – Online Training Overview: Defined Failure Investigation and Root Cause Analysis is a major tool in product complaint, non-conformance, and OOS failure investigations, and hazard analysis / risk management and mitiga… Organized by GlobalCompliancePanel | Type: webinar, healthcare, medical, device, pharmaceutical, clinical
May 7, 2013 from 10am to 11:30am – United States Overview: This webinar covers the fundamentals of 21 CFR Part 11, software validation, and computer system validation. It provides details for company compliance including GAMP, qualification, and va… Organized by GlobalCompliancePanel | Type: webinar, healthcare, medical, device, pharmaceutical, clinical
May 2, 2013 from 10am to 11:30am – Online Training Overview: There is a need to implement an adequate formal level of change control during engineering projects (referred to as an Engineering Change Control) after the approval of the equipment/system… Organized by John Robinson | Type: webinar, healthcare, medical, device, pharmaceutical, clinical
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