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Global Medical Device Laws and Regulations: US, EU, and Canada

ComplianceOnline

Tuesday, June 18, 2013 from 10:00 AM to 11:30 AM (PDT)

Palo Alto, CA

Global Medical Device Laws and Regulations: US, EU, and...

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Ticket Type Sales End Price Fee Quantity
Online Registration Ended $299.00 $17.44

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Event Details

This training on global medical device regulations will discuss the regulatory framework for medical devices in US, EU and Canada. It will outline systematic methods to identify and meet regulatory requirements and streamline the regulatory process in these countries.

Why Should You Attend:

Global regulations of medical devices are rapidly evolving, integrating the regulatory systems of the advanced medical device regulations. To be able to achieve sustainability and to remain sustainable and competitive in global medical device markets, it is necessary to streamline the regulatory process. To do so, we should understand differences in regulatory frameworks (regulatory requirements and compliance) in a sustainable and effective way.

This 90-minute training will discuss medical device laws and regulations in the USA, EU and Canada. It is intended to guide you through to understand and accurately interpret applicable laws and regulations governing medical devices in the above global countries. The presenter will guide participants from the medical device industry to streamline their business planning and regulatory strategy in these global markets.

Areas Covered in the Webinar:

  • Medical device laws and regulations in the US, EU and Canada.
  • Definitions
  • Regulatory framework for medical devices in the US, EU, and Canada
  • Device classification
  • Regulatory requirements for medical devices including in vitro diagnostic devices in the US, EU and Canada.
  • Contents of a 510(k) and PMA in US
  • Contents of a technical file and design dossier in EU
  • Content of a medical device license application in Canada
  • How to identify and meet the regulatory requirements.
  • How to establish and maintain systematic methods to meet the regulatory requirements.
  • How to streamline the regulatory process
  • Instructor’s unique regulatory guide.

 

 

For Registration:

http://www.complianceonline.com/ecommerce/control/trainingFocus/~product_id=702842?channel=Eventbrite

Have questions about Global Medical Device Laws and Regulations: US, EU, and Canada? Contact ComplianceOnline

When & Where



Online Webinar
2600 E. Bayshore Road
Palo Alto, CA 94303

Tuesday, June 18, 2013 from 10:00 AM to 11:30 AM (PDT)


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Organizer

ComplianceOnline

At ComplianceOnline, we are focused on :

 

  • Enhancing global compliance, creating a world where quality and compliance professionals, regulators, and government agencies come together to help the world comply with the intent and the spirit of laws, policies and mandates, ensuring continuous improvement in global operations, quality & safety.
  • Making sure that we are responsible corporate citizens helping our constituents build a more responsible enterprise, one which operates with high quality , under a code of ethics, and with process discipline to ensure greater shareholder returns.
  • Keeping things simple and straight forward , so that we all can indeed improve the quality of our processes, our work, our businesses and enhance compliance globally.
  • Being inclusive, giving the process experts ( & novices! ), compliance professionals, quality champions, and regulatory agencies a voice so that all of us can contribute and make a difference.

 

 

 

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