All John Robinson clinical Events (85)

Introduction to SPC (Statistical Process Control)

March 20, 2014 from 10am to 11:30am – Online Event Overview: Manufacturing involves an attempt to produce items that as closely as possible meet design specifications (e.g., size, strength, etc.). However, all production processes exhibit variation -… Organized by John Robinson | Type: webinar, pharma, medical, clinical, health
Risk Management for Medical Devices - ISO 14971 - Webinar by GlobalCompliancePanel

March 20, 2014 from 10am to 11:15am – Online Event Overview: This course provides the attendees with an overview of ISO 14971:2007 and implementation tips for an effective system for managing risk. We provide an overview using flow charts that shows… Organized by John Robinson | Type: webinar, pharma, medical, clinical, health

Japan - Regulatory Filing Requirements and Compliance Processes for Life Sciences

March 19, 2014 from 10am to 11:30am – Online Event Overview: This course specifically focuses on the overall regulatory compliance requirements and procedures for Pharmaceuticals, Medical Devices, Biologics and Combination Products in Japan. The cour… Organized by John Robinson | Type: webinar, pharma, medical, clinical, health

Drafting a Software V&V Documentation Package and Protocol

March 18, 2014 from 10am to 11am – Online Event Overview: The verification and validation of medical software is coming under increased scrutiny by the U.S. FDA. This webinar will address the use of the FDA, DAMP, and other applicable industry sof… Organized by John Robinson | Type: webinar, pharma, medical, clinical, health
Conducting Successful Product Complaint Investigations

March 18, 2014 from 10am to 11am – Online Event Overview: This webinar will provide valuable assistance and guidance to the life sciences manufacturers engaged in various aspects of product complaint investigations. An effective complaint handling… Organized by John Robinson | Type: webinar, pharma, medical, clinical, health

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