ComplianceOnline

Introduction to FDA and EU Medical Device Submission

Instructor: Charles H Paul
Product ID: 705065
  • Duration: 60 Min
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Read Frequently Asked Questions

This webinar will overview each critical aspect of the FDA submissions process to include 510(k) and PMA) and contrast those key steps to those of the EU Medical Device Directives Submissions process.

Why Should You Attend:

It is imperative that a unified regulatory strategy be established by manufacturers to ensure that their designed and developed medical devices are approved for their target markets.

This webinar will address those specific aspects of the regulatory climate that must be properly applied and addressed to achieve a successful submission and approval. Requirements for submissions and approvals differ from country to country however the core submissions requirements are very similar. This webinar will spotlight this differences and focus upon the required quality system elements that must be addressed, provide an overview of the FDA premarket and EU Medical Device Directives submissions processes, and discuss how devices are classified.

Areas Covered in the Webinar:

  • Medical device classifications
  • 510(k) and PMA
  • Current EU Directives
  • Intended use
  • Indications for use
  • IDEs, HUDs
  • Quality system certification
  • Product certification
  • Technical files and design dossiers

Who Will Benefit:

This webinar will provide valuable assistance to all personnel in:

  • Manufacturing
  • Engineering
  • Quality Assurance
  • Production
  • Regulatory submissions
  • Research & Development
Instructor Profile:
Charles H. Paul

Charles H. Paul
President, C H Paul Consulting Inc

Charles H. Paul is the President of C. H. Paul Consulting, Inc. – A regulatory, training, and technical documentation consulting firm. Charles is a management consultant, instructional designer and regulatory consultant and has led C. H. Paul Consulting, Inc. since its inception over 25 years ago. He regularly consults with Fortune 500 pharmaceutical, medical device, and biotechnology firms assisting them in achieving human resource, regulatory, and operational excellence. He is a regular presenter of webinars and on-site seminars in a variety of related subjects from documentation development to establishing compliant preventive maintenance systems.

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Refund Policy

Registrants may cancel up to two working days prior to the course start date and will receive a letter of credit to be used towards a future course up to one year from date of issuance. ComplianceOnline would process/provide refund if the Live Webinar has been cancelled. The attendee could choose between the recorded version of the webinar or refund for any cancelled webinar. Refunds will not be given to participants who do not show up for the webinar. On-Demand Recordings can be requested in exchange.

Webinar may be cancelled due to lack of enrolment or unavoidable factors. Registrants will be notified 24hours in advance if a cancellation occurs. Substitutions can happen any time.

If you have any concern about the content of the webinar and not satisfied please contact us at below email or by call mentioning your feedback for resolution of the matter.

We respect feedback/opinions of our customers which enables us to improve our products and services. To contact us please email customercare@complianceonline.com call +1-888-717-2436 (Toll Free).

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