Special Considerations during Medical Device Design: Dos and Don'ts

Attend this webinar to learn do's & don'ts of medical device design process and also methods with which a company can capture most of the requirements.
By: OnlineCompliancePanel LLC
 
FREMONT, Calif. - Feb. 5, 2015 - PRLog -- Instructor:
Dev Raheja

Description:


In the past, the designer was in charge of everything that could go wrong in the product performance. Today product's manufacturing processes, supply chain controls, and product users have become disengaged in many companies: therefore most design engineers are far removed from many things going wrong. The most efficient way to prevent recalls is to identify as many potential problems as early as possible related to safety, reliability, durability, and efficacy using the best practices. This needs to be done before approving specifications.

Why Should you Attend:

No person can capture all the requirements not even a team of intelligent cross functional members. This webinar will discuss about the structured methods with which a company can capture most of the requirements. Insufficient knowledge will lead to insufficient device performance. Therefore entire product development team should take advantage of this webinar.

Objectives of the Presentation:

Learning objectives of this webinar are:
Right things you must always do
Conducting Requirements Analysis to Identify Missing Requirements
Conducting Preliminary Hazard Analysis (PHA) to Assess Risks
Negative requirements Analysis for Worst Case Scenarios
Specification for Safety, Durability, and Reliability
Specification for User Interface and Usability
Specification for Maintainability
Designing for hazard-free maintenance
Specification for Prognostics
Specification for Safe Software
Mitigating risks using world class practices
Installation qualification, operational qualification
Performance qualification
Specification for Safety, Durability, and Reliability
Specification for User Interface and Usability
Designing to Forgive User Errors
Specification for Prognostics
Independent verification and validation
Wrong things you must avoid
Group Think process
Myopia of knowledge
Inefficient team management
Approving specifications without challenge
Mitigating risks using outdated practices
Accepting costly solutions
Insufficient control on residual risks

Who can Benefit:

All Engineering managers and Engineers
Entire QA staff
Entire Regulatory staff
Device Maintenance staff
Marketing staff

Quick Contact:

http://www.onlinecompliancepanel.com/ecommerce/webinar/~p...

Toll free: +1-510-857-5896

Email: webinar@onlinecompliancepanel.com

OnlineCompliancePanel LLC,

38868 Salmon Ter,

Fremont, CA 94536, USA

Contact
Compliance Panel
***@gmail.com
End
Source:OnlineCompliancePanel LLC
Email:***@gmail.com
Tags:Medical Device Design, Medical
Industry:Education
Location:Fremont - California - United States
Subject:Events
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