The Cutting Edge of Medical Technology Content, Community & Collaboration
July 6, 2017 at 9am to July 7, 2017 at 6pm – San Diego, CA Course "Audit Like the FDA - What you need to know for a truly effective internal audit program" has been pre-approved by RAPS as eligible for up to 12 credits towards a participant's RAC recertifica… Organized by NetZealous DBA as GlobalCompliancePanel | Type: online, healthcare, training, courses
July 6, 2017 at 9am to July 7, 2017 at 6pm – Washington, DC Course "21 CFR Part 11 compliance for software validation and SaaS/Cloud" has been pre-approved by RAPS as eligible for up to 12 credits towards a participant's RAC recertification upon full completi… Organized by NetZealous DBA as GlobalCompliancePanel | Type: online, healthcare, training, courses
July 6, 2017 at 8:30am to July 7, 2017 at 4:30pm – New York City, NY Overview: This course covers a very broad range of topics from worker classification, to employee classification, to establishing methods and rates of pay, what must be included in the rate of pay, h… Organized by NetZealous DBA as GlobalCompliancePanel | Type: online, healthcare, training, courses
June 1, 2017 at 9am to July 28, 2017 at 6pm – INTERCONTINENTAL HONG KONG GlobalCompliancePanel’s seminars are a wonderful opportunity for professionals in the regulatory compliance areas to understand the latest happenings and updates in the regulatory compliance areas an… Organized by NetZealous DBA as GlobalCompliancePanel | Type: online, healthcare, training, courses
April 9, 2015 at 9am to April 10, 2015 at 6pm – DoubleTree by Hilton Hotel Los Angeles Downtown Overview: This webinar will cover issues concerning industrial / scientific labs describing the differences between manufacturing and scientific labs. It will also discuss how management relates to t… Organized by GloalCompliancePanel | Type: food, fda, medical, device, aerospace, navy, and, defence, healthcare
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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