The Cutting Edge of Medical Technology Content, Community & Collaboration
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
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
April 9, 2015 at 9am to April 10, 2015 at 6pm – DoubleTree by Hilton Hotel Los Angeles Downtown Overview: Writing SOPs or procedural documents can be challenging at times. However, writing SOPs is overall a straightforward process. However, enforcing what you already created and implemented in… Organized by GlobalCompliancePanel | Type: food, fda, medical, device
April 9, 2015 at 9am to April 10, 2015 at 6pm – Los Angeles, California, United States Overview: 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 training,… Organized by GlobalCompliancepanel | Type: food, health, care, medical, device, mining, aerospace, and, navy, fda
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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