Past Events (3,027)

edical Device Postmarketing Vigilance Reporting: Update and Expectations for Manufacturers - Webinar By GlobalCompliancePanel

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

Medical Device Design Control - Webinar By GlobalCompliancePanel

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
CAPA, Failure Investigation and Root Cause Analysis to Meet FDA Expectations - Webinar By GlobalCompliancePanel

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

Common Problems with Software Validation Processes - Webinar By GlobalCompliancePanel

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

Effective and Compliant Change Control Management - Before, During and After Validation - Webinar By GlobalCompliancePanel

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

"NextMed / MMVR20" Conference

February 20, 2013 to February 23, 2013 – San Diego Marriott Mission Valley, San Diego, California The Call for Presentations is now open for "NextMed/MMVR20". Submission deadline is July 15, 2012. Details at NextMed.com . For two decades, scientists and engineers, physicians and other care provi… Organized by James D. Westwood | Type: conference

CAPA Systems for Medical Device Manufacturers

October 4, 2012 at 9am to October 5, 2012 at 5pm – Boston Marriott Copley Place Course Description: Implementing an effective system for corrective action and preventive action can be a major challenge. FDA illustrates the point in its published information on Warning Letters. F… Organized by Referral | Type: medical, training

Decommissioning a Medical OEM Molding Operation and Transferring to a Contract Manufacturer

September 27, 2012 from 10am to 11am – Online Event This webinar will provide processes and procedures to all medical device companies that are thinking of transferring equipment, molds, dies, systems and processes to contract manufacturers. It will f… Organized by Referral | Type: medical, training
Verification and Validation – Product, Equipment, Software and QMS

September 27, 2012 at 8:30am to September 28, 2012 at 4:30pm – Grand Hyatt San Francisco Course Description: Develop / review a company's Master Validation Plan for major cGMP deficiencies. Address the U.S. FDA's newer and tougher regulatory stance. One major failing is lack of sufficien… Organized by Referral | Type: medical, device, training