Past Events (3,027)

Post Market Surveillance for Medical Devices

September 26, 2012 from 8am to 9:30am – 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 Referral | Type: medical, training

10 Steps to Success for Effective Corrective And Preventive Actions (CAPA)

September 25, 2012 from 9am to 11am – Online Event This 120-minute webinar will explain all elements of CAPA process steps as required by ISO and regulatory agencies. In addition, it will be presented in a practical and proven manner, which can be im… Organized by Referral | Type: medical, training
17th Annual CyberPsychology and CyberThearpy Conference

September 25, 2012 to September 28, 2012 – Brussels, Belgium The Interactive Media Institute, in collaboration with the Virtual Reality Medical Institute, is pleased to announce the International Association of CyberPsychology, Training, & Rehabilitation's… Organized by International Association of CyberPsychology, Training & Rehabilitation | Type: conference

Creating a Good Design History File for Audit Success

September 21, 2012 from 10am to 11am – Online Event This webinar will cover the basics on how to maintain a good Design History File that will help a manufacturer during a regulatory compliance audit. Why Should You Attend: A Design History File (DHF)… Organized by Referral | Type: medical, device, training

Medical Device CE Mark - Required to Sell in European Union Market

September 13, 2012 from 10am to 11am – Online Event This webinar on selling medical devices in the European Union (EU) will immensely benefit companies wishing to penetrate the EU market for medical devices or sharpen their skills. It will provide pra… Organized by Referral | Type: medical, device, training
Global Medical Device Regulations Seminar

September 13, 2012 at 9am to September 14, 2012 at 4pm – Hyatt Regency Minneapolis Course Description: At this workshop, Dr. David Lim will walk you through to get familiar with the medical device regulations in the following twelve (12) countries.United States, EU, Canada,Argentin… Organized by Referral | Type: medical, device, seminar

Implement Parametric Release in EO Sterilization - A Practical Approach

September 11, 2012 from 10am to 11am – Online Event This webinar will present a practical approach for implementing parametric release in EO sterilization. We will discuss the cycle validation and other requirements for implementation of parametric re… Organized by Referral | Type: medical, device, compliance
Process Verification and Validation Planning and Execution

September 11, 2012 from 10am to 11:30am – Online Event This 90-minute session on risk-based verification and validation planning will discuss "must have" elements from the U.S. FDA cGMP, ICH Q9 and ISO 14971 for hazard analysis and product risk managemen… Organized by Referral | Type: medical, training
Understanding and Applying Risk Management

September 11, 2012 from 9am to 11am – Online Event This 120-minute webinar will cover best practices and standardized processes, outlined in ISO 14971, for managing risk in medical devices. You will learn from the shared experience and examples provi… Organized by Referral | Type: medical, device, training

How to Investigate Environmental Monitoring Excursion Limits

September 6, 2012 from 10am to 11am – Online Event This environmental monitoring training will review the best practices for setting environmental monitoring alert and action levels for viable and non-viable data including product bioburden. In addit… Organized by Referral | Type: medical, training