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Why are these Webinars so valuable?

What do you get with this Webinar?

What do Registrants say about RAQA Webinars?

How about a private webinar?

AVAILABLE WEBINARS:

Internal Audit Process

Internal Auditor Training

Regulatory Affairs/Quality Assurance
(RAQA) Tune Up!


Bullet-proof Medical Device Design

New Environmental
Regulations


Risk Management, ISO 14971 and More!

Canadian Medical Device Regulations

European Union Medical Device Regulatory Update

Preparing for USFDA Inspections/Notified Body Audits

Introduction to ISO 13485 Quality Management Systems

Technical (STED) Files

Approved Suppliers

CAPA (Corrective and Preventative Actions)

Labelling and Instructions for Use

Power of Continuous Improvement

Contact us

Webinars – the perfect way to stay current on key regulatory and quality system requirements without ever leaving your office. All you need is a computer, telephone and Internet connection. When your schedule is simply too demanding to travel three days for a one day educational event, a webinar is what you need. No travel, easy to use, cost effective yet filled with timely information and solutions that work for regulatory and quality system issues that are key to growing your market share. There is ample time allotted for participants to ask question and receive answers, explore example documents, review specific requirements and you even have expert contributors so you can compare and contrast answers from different perspectives. You can educate your whole team with one low fee!

Registration is limited to ensure a personalized learning environment including a lively question and answer session, reviewing sample documents and discussion of case studies.

 

This year’s webinar schedule:

    19 February, 1 pm Eastern
    • Risk Management, ISO 14971 and more!
    •  

    26 February, 1 pm Eastern
    • Bullet-proof Medical Device Design
    •  

  • 11 March, 1 pm Eastern
    • Canadian Medical Device Regulations (CMDR)
    •  

    18 March, 1 pm Eastern
    • European Union Medical Device Regulatory Update
    •  

  • 20 March, 1 pm Eastern
    • Preparing for USFDA Inspections/Notified Body Audits
  • 25 March, 1 pm Eastern
    • Introduction to ISO 13485 Quality Management Systems

     

  • 8 April, 1 pm Eastern
    • Labelling and Instructions for Use
  • 22 April, 1 pm Eastern
    • Technical (STED) Files
    •  

    7 May, 1 pm Eastern
    • RAQA Tune Up

     

  • 14 May, 1 pm Eastern
    • Internal Audit Process
    •  

    21 May, 1 pm Eastern
    • Internal Auditor Training

     

  • 3 June, 1 pm Eastern
    • Approved Suppliers
    •  

  • 10 June, 1 pm Eastern
    • Environmental Regulations and the effect they will have on medical device manufacturing

     

  • 17 June, 1 pm Eastern
      Preparing for USFDA Inspections and Notified Body Audits

     

  • July 2008 - Have a great summer!
  •  

  • 19 August, 1 pm Eastern
    • Internal Audit Process

     

  • 26 August, 1 pm Eastern
    • Internal Audit Training

     

  • 9 September, 1 pm Eastern
    • RAQA Tune Up

     

  • 16 September, 1 pm Eastern
    • Bullet Proof Medical Device Design

     

  • 23 September, 1 pm Eastern
    • CAPA (Corrective and Preventative Actions)

     

  • 7 October, 1 pm Eastern
    • Canadian Medical Device Regulations

     

  • 21 October, 1 pm Eastern
    • European Union Medical Device Regulatory Update

     

  • 28 October, 1 pm Eastern
    • Technical (STED) Files

     

  • 6 November, 1 pm Eastern
    • Preparing for USFDA Inspections and Notified Body Audits

     

  • 18 November, 1 pm Eastern
    • Internal Audit Process

     

  • 20 November, 1 pm Eastern
    • Internal Auditor Training

     

  • 11 December, 1 pm Eastern
    • RAQA Tune Up

 

 

 

 

Webinar Schedule

Webinar Schedule


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