LIVE WEBINAR 2023 - Design Control for Medical Devices and Combination Products
Date2023-05-18
Deadline2023-05-17
VenueOnline Event, USA - United States
KeywordsWebinar; Livewebinar; Livetraining
Websitehttps://bit.ly/3WaGhiQ
Topics/Call fo Papers
This Webinar will outline the basics of design control for medical devices and the device part of a combination product. Failure to develop these products under design control may result in a product that is not suited for the intended market or failure of approval to market from regulatory agencies.
WHY SHOULD YOU ATTEND?
This Webinar will outline the basics of design control for medical devices and the device part of a combination product. The webinar will cover the basics of design control and the overall flow of the design control process. It will also cover the aspects of inputs into the design control process (design inputs) and how inputs are key to the entire process. Understanding the process of design control is essential for the successful development of medical devices as well as a regulatory requirement.
AREA COVERED
Overview of design control
Need for design controls in device design
Regulatory requirements
Design inputs: User Needs
Design inputs: Product Requirements
Next steps in design inputs
LEARNING OBJECTIVES
Understand the need for design control in product development
Understand the regulatory requirements from both the FDA and CE mark perspectives
Learn the flow of design control
Understand user needs, the start of design control
Understand the translation of user needs to product requirements
Next steps
WHO WILL BENEFIT?
Quality professionals
Regulatory Affairs Professionals
R&D Scientists
Production Personnel and Technical Support Personnel.
WHY SHOULD YOU ATTEND?
This Webinar will outline the basics of design control for medical devices and the device part of a combination product. The webinar will cover the basics of design control and the overall flow of the design control process. It will also cover the aspects of inputs into the design control process (design inputs) and how inputs are key to the entire process. Understanding the process of design control is essential for the successful development of medical devices as well as a regulatory requirement.
AREA COVERED
Overview of design control
Need for design controls in device design
Regulatory requirements
Design inputs: User Needs
Design inputs: Product Requirements
Next steps in design inputs
LEARNING OBJECTIVES
Understand the need for design control in product development
Understand the regulatory requirements from both the FDA and CE mark perspectives
Learn the flow of design control
Understand user needs, the start of design control
Understand the translation of user needs to product requirements
Next steps
WHO WILL BENEFIT?
Quality professionals
Regulatory Affairs Professionals
R&D Scientists
Production Personnel and Technical Support Personnel.
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Last modified: 2023-05-17 15:24:44