Webinar Information


ISO 13485:2016 – Are your suppliers ready?


ISO 13485:2016 – Are your suppliers ready?, Aurora, Colorado, United States
Webinar Title
ISO 13485:2016 – Are your suppliers ready?
Event Type
Webinar
Webinar Date
14-06-2018
Last Date for Applying
14-06-2018
Location
Aurora, Colorado, United States

Publish / Maintain / Marketing / Hosted By
Organization Name / Organize By
Training Doyens
Organizing/Related Departments
Cross Industry Functions
Organization Type
Organization/Company
Webinar Category
Both (Technical & Non Technical)
Webinar Level
All (State/Province/Region, National & International)
Related Industries

Education/Teaching/Training/Development

Business Development

Economics

Accounting/Financial/Banking/Insurance

Export/Import

Location
Aurora, Colorado, United States

OVERVIEW

This 1-hour session will provide the attendees with experience gained in providing transition assistance to medical device companies over the last 2 years. What constitutes a written quality agreement for outsourcing? What is the risk-based approach for supply chain management?

WHY SHOULD YOU ATTEND

All organizations that are part of the medical device supply chain are required to establish a quality management system to ISO 13485. The transition period is coming to an end for the third edition of ISO 13485 and certifications to the second edition will expire by March 2019. If you haven’t completed the transition your organization may not be able to market devices in 2019 or you may have corrective actions forced on you by your customers. This webinar will provide you with practical actions you can take to ensure your certification to this new edition of the standard is obtained.

AREAS COVERED

  • Role of the organization
  • Risk-based approach
  • Outsourcing
  • Criteria for supplier selection and monitoring
  • Risk-based controls for supplier management

LEARNING OBJECTIVES

The transition period for this quality management system standard is coming to an end soon (February 2019). One of the key clarifications is the requirements for outsourcing as well as the selection and monitoring of suppliers. Have you prepared your supply chain for these changes? Do you expect conformance with ISO 13485 or ISO 9001?

WHO WILL BENEFIT

  • Supplier Management
  • Auditors
  • SMEs doing the work
  • Quality assurance
  • Regulatory Professionals
  • Biostatistics
  • Data Management

For more detail please click on this below link:

https://bit.ly/2rYoTjD

Email: support@trainingdoyens.com

Toll Free: +1-888-300-8494

Tel: +1-720-996-1616    

Fax: +1-888-909-1882

 

 

Others Details

Understand the various requirements of ISO 13485 and learn about the practical actions you can take to ensure your certification to the new edition of the standard is obtained.

Registration Fees
Not Mention
Registration Ways
Email
Phone
Website
Other
Address/Venue
Training Doyens 26468 E Walker Dr,Aurora, Colorado  Pin/Zip Code : 80016-6104
Landmark
Colorado
Official Email ID
support@trainingdoyens.com
Contact
Training Doyens

26468 E Walker Dr,Aurora, Colorado

support@trainingdoyens.com

   +1-720-996-1616