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Webinar On FDA proposed changes to ISO 13485: 2015 and Medical Devices Quality Management Systems

 
  December 09, 2014  
     
 


Compliance Trainings, Online
2015-01-30


On Going Christmas Offers: Offer valid till 1 st January 2015

1. Register an attendee for Single Live:

Get 10% of on every Registration

First 10 attendees will receive recording Access to the webinar for No Additional Cost

For Coupon Code call customer support:  416-915-4458

2. Register your Group for Corporate Live:

Get 15% of on every Registration

Every group registrant will receive Recording Access to the webinar for No Additional Cost

For Coupon Code call customer support: 416-915-4458

3. Unlimited viewing for 4 days

4. The discounted amount will appear after entering the Coupon Code in the Secure Check Out Page

Description :

ISO 13485:2015 - What’s coming? Understand proposed changes being worked on by the ISO technical committee for updating the ISO 13485:2003. Awareness of the current requirements and proposed changes will facilitate your preparing in advance and navigating your way through the harmonized international arena to expand your product marketing strategies.

Areas Covered in the Session :

You will gain a thorough understanding of:

Requirements of ISO 13485

How to carefully attend to every aspect of the related biomedical standards

Document control

Purchasing Controls

Production controls

CAPA

Identification and Traceability

Upcoming changes ISO 13485:2015

How ISO 13485 differ from FDA QSR 21 CFR 820 requirements

Regulatory expectations of other major growing geographies in the world

Who Will Benefit:

A must attend webinar for Managers, Supervisors, Leads, Specialists, Engineers and Groups in Department of:

Quality Assurance

Regulatory Affairs

Research & Development

Quality Control

Supplier Management

Documentation

Production

Internal Auditors

Quality Auditors

Supplier Auditors

Operations

Manufacturing

Suppliers to medical device industry

Price tags:

Live

Single Live : For One Participant

$ 249

Corporate Live : For Max. 10 Participants

$ 899

Recording

Single REC : For One Participant - Unlimited Access for 6 Months

$ 299

For more information and enquiries contact us at

Compliance Trainings

5939 Candlebrook Ct, Mississauga, ON L5V 2V5, Canada 
Customer Support : #416-915-4458 
Email : support@compliancetrainings.com

For more information about this event please visit

https://compliancetrainings.com/SiteEngine/ProductDetailView.aspx?id=MD1093 

 
 
Organized by: Compliance Trainings
Invited Speakers:

Speaker Profile

Meena Chettiar is a certified instructor for ASQ learning institute for CBA and an adjunct instructor for Medical Technology Quality graduate program for St. Cloud State University in Minnesota. Meena is a coauthor of the CBA (Certified Biomedical Auditor) Primer for the Quality Council of Indiana. 

 
Deadline for Abstracts: 2015-01-30
 
Registration:

https://compliancetrainings.com/siteengine/Login.aspx

E-mail: suzzane.d@compliancetrainings.com
 
   
 
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