Events, Appearances and Conferences

 

If you’re attending an industry tradeshow or conference, look for LNE/G-MED America. Our technical experts are often called on to present educational sessions, and we regularly support selected shows by exhibiting.

Most importantly, we attend industry events so we can touch base with clients and meet other professionals who want to demonstrate their quality and comply with international regulation. Contact us to request a free on-site consultation to address all of your questions.  

Here’s our upcoming appearance schedule:

May 21-24, 2013
Hospitalar 2013, São Paulo, Brazil

LNE/G-MED will exhibit at Hospitalar 2013, the international trade show of health and medical products, equipment, services, and technology, in São Paulo, Brazil, from May 21-24.  Come see us at Booth 94 in Aisle 1 in the Green Pavilion.  To reserve your free meeting time, email us at certfication(at)lne-gmed.com  or use our contact form.  

July 8-12
TRAINING – EU Medical Device Regulatory Essentials

The essentials of a medical device’s European market access strategy are the regulatory requirements, the technical documentation, and the risk management and vigilance systems for the device.  The proper understanding of these requirements, and how to apply them to a device, is key to CE Marking and continued market access for your device.  
LNE/G-MED offers EU Medical Device Regulatory Essentials, a week-long course in understanding and applying these requirements for CE Marking and continued market access.  This course is a must for any new Regulatory or Quality professional, or even experienced professionals wishing to brush up on their skills or learn more about different regulatory requirements.  
  • Where: Silver Spring Innovation Center, Silver Spring, MD
  • When: July 8-12
  • What: EU Medical Device Regulatory Essentials
  • Price: $1799
Register now    

July 22-24
TRAINING – Medical Device Sterilization (EtO, Radiation) and Cleaning

Sterilization (EtO and Irradiation) and Cleaning Processes Validation is a comprehensive, three-day course covering the standards, validation methods, and best practices for cleaning and sterilizing medical devices.  This program will provide participants with a variety of knowledge and skills:
  • Gain a deep understanding of the differences between ethylene oxide and irradiation sterilization processes, their modes of action and their influence factors;
  • Learn methodology as well as the technical and documentary tools required to validate, implement, control, and audit the cleaning and sterilization processes by ethylene oxide or irradiation;
  • Manage and control contract and in-house cleaning and sterilization activities and satisfy regulatory requirements.
Course participants will gain an in-depth understanding of the European approach, from definition of key terms to the motivations of authorities which help illustrate the rationale of particular requirements.
Register now    
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