The Cutting Edge of Medical Technology Content, Community & Collaboration
July 31, 2014 at 9am to August 1, 2014 at 6pm – WILL BE ANNOUNCED SOON Overview: This course provides an overview of international medical device regulations. Beginning with a discussion of the similarity of global requirements, including both voluntary and mandatory st… Organized by GlobalCompliancePanel | Type: seminar, pharma, medical, clinical, health, compliance, regulatory, fda
July 30, 2014 from 10am to 11am – Online Event Overview: All life science businesses are required to maintain their Quality Management System (QMS) processes in a state of control, via controlled documents and objective evidence in the form of re… Organized by GlobalCompliancePanel | Type: seminar, pharma, medical, clinical, health, compliance, regulatory, fda
July 30, 2014 from 10am to 11am – Online Event Overview: What is a combination product? What are some examples of combination products? How are combination products assigned for review? Where can I find guidance for how master files can be used i… Organized by GlobalCompliancePanel | Type: seminar, pharma, medical, clinical, health, compliance, regulatory, fda
July 29, 2014 from 10am to 11am – Online Event Overview: Supplier qualification and assessment is required in both the QSR regulations and ISO standards.Many companies spend a great deal of time and money in pursuit of compliance with this. Many… Organized by GlobalCompliancePanel | Type: seminar, pharma, medical, clinical, health, compliance, regulatory, fda
July 29, 2014 from 10am to 11am – Online Event Overview: Software's level of complexity and use is expanding at exponential levels. Likewise the potential risks to health follow suit. Problems with software create a number of different hurdles. S… Organized by GlobalCompliancePanel | Type: seminar, pharma, medical, clinical, health, compliance, regulatory, fda
July 24, 2014 at 9am to July 25, 2014 at 6pm – WILL BE ANNOUNCED SOON The Problem: Computer Systems Validation (CSV) also known as Software Validation is all-pervasive in the Life Sciences Industry. It is a requirement of all the predicate rules, as well as 21 CFR 11 a… Organized by GlobalCompliancePanel | Type: seminar, pharma, medical, clinical, health, compliance, regulatory, fda
July 24, 2014 at 9am to July 25, 2014 at 6pm – DoubleTree by Hilton Hotel San Francisco Airport Overview: The 2-day seminar begins with an examination of ISO and FDA regulations and guidelines regarding the use of statistics. Basic vocabulary and concepts are then reviewed and discussed. The fl… Organized by GlobalCompliancePanel | Type: seminar, pharma, medical, clinical, health, compliance, regulatory, fda
July 22, 2014 from 10am to 11am – Online Event Overview: This interactive webinar teaches how to determine and document risk in a process in order to reduce validation time and ensure compliance.What makes this session unique are the real life ex… Organized by GlobalCompliancePanel | Type: seminar, pharma, medical, clinical, health, compliance, regulatory, fda
July 17, 2014 from 10am to 11am – Online Event Overview: This webinar is intended to share 510(k) hurdles and good practices, in particular, how to prepare a 510(k) in a sufficiently adequate manner with increased quality to expedite review proce… Organized by GlobalCompliancePanel | Type: seminar, pharma, medical, clinical, health, compliance, regulatory, fda
July 17, 2014 at 9am to July 18, 2014 at 6pm – WILL BE ANNOUNCED SOON Overview: This session is designed to provide intensive, two-day training in HIPAA compliance, including what's new in the regulations, what's changed recently, and what needs to be addressed for com… Organized by GlobalCompliancePanel | Type: seminar, pharma, medical, clinical, health, compliance, regulatory, fda
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