All ComplianceOnline medical Events (19)

Post Market Surveillance for Medical Devices

February 27, 2014 from 10am to 11:30am – Online Event This 90-minute webinar covers all aspects of post market surveillance (PMS) for medical devices. It will direct you to the specific documents for the detailed information you need for an effective po… Organized by ComplianceOnline | Type: medical

Automating Laboratory Assays For the Bench

February 25, 2014 from 10am to 11am – Online Event This webinar on automating laboratory assays will teach you how to translate an assay that is performed manually to one that is fully automated, with high quality and with proper validation and quali… Organized by ComplianceOnline | Type: medical

Navigating through Maze of In-vitro Diagnostics (IVD) Regulations: A systematic approach from Regulatory Strategy to Regulatory Approvals in U.S./Europe/Canada: 2-day In-Person Seminar

February 20, 2014 at 8:30pm to February 21, 2014 at 4:30pm – Double Tree San Diego Downtown Course Description: In-vitro Diagnostics (IVD) products provide critical information on patient’s health condition, based on which the healthcare provider develops and administers treatment plan. Alt… Organized by ComplianceOnline | Type: medical

Understanding the FDA ''Refuse to Accept'' guidance to avoid administrative rejection of your 510(k)

February 19, 2014 from 10am to 11am – Online Event The webinar will familiarize participants with the FDA's Refuse to Accept Policy for medical device 510(k)’s and help you ensure that your 510(k) application is not rejected for lack of administrativ… Organized by ComplianceOnline | Type: medical
Understanding the FDA ''Refuse to Accept'' guidance to avoid administrative rejection of your 510(k)

February 19, 2014 from 10am to 10pm – Online Event The webinar will familiarize participants with the FDA's Refuse to Accept Policy for medical device 510(k)’s and help you ensure that your 510(k) application is not rejected for lack of administrativ… Organized by ComplianceOnline | Type: medical

The Sunshine Act Reporting for Clinical Trials

December 19, 2013 from 10am to 11am – Online Event This webinar will discuss the disclosure requirements for clinical investigators under the Sunshine Act. It will discuss the details of the processes; provide templates for reporting formats; and tim… Organized by ComplianceOnline | Type: online, medical, event

FDA's Oversight of Mobile Medical Applications (''apps'') for Use on Smartphones and Similar Mobile Devices

December 18, 2013 from 10am to 11:30am – Online Event This training on FDA regulation of mobile medical applications is designed to provide attendees with an overview of the U.S. Food and Drug Administration's oversight of certain medical and healthcare… Organized by ComplianceOnline | Type: medical

Information on Cyber Security to Include in Medical Device Submissions

December 5, 2013 from 10am to 11:15am – Online Event This training will focus on the new draft guidance document recently released by the FDA on ensuring medical device cybersecurity. Attendees will gain insight into the security activities and documen… Organized by ComplianceOnline | Type: medical, related