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Live -Webinar 2014 - Secrets of Successful Medical Device Product Development Process
Topics/Call fo Papers
DESCRIPTION
We will give you the steps and information to develop a medical device product. The documentation discussed can also be used and is often requested by the FDA and required by many ISO procedures for controlling the design process. We will discuss why certain steps are so important in the design process and that many steps are not just wasted time and paperwork. The process is a methodical approach that can be used with almost any product development process from concept to production. The speaker has a proven track record of successful products and many of them have been on the market longer than the 5 or 10 year expected product life cycle. The speaker has 20 granted patents and over 83% percent of them have been commercialized and using this process.
Why should you attend :
The medical device development process can be long and costly, but not if you follow some proven guidelines and steps. Sometimes projects are continuously pushed forward without doing proper reviews to see if the project warrants going to the next step. The sooner this process is done the better as it saves time and money. Good products also need to be completed faster and with less capital to beat the competition to market and beat them with a good quality product that needs little to no revisions and one that receives very few to no complaints from the customer. We will teach you the secrets of turning your medical device ideas into profit making products, which are the same steps that can also enable you to see why the project should be cancelled.
Areas Covered in the Session:
How to start a development project.
Patent search
Putting together a comprehensive systems requirement document.
1-10-100 Rule
Market research and customer needs
Design in quality & manufacturability
Prototype & testing
Production tooling
Qualification, Validation, & Verification
Trace matrix
Technical File & Regulatory Documentation
Who will benefit: (Titles)
Medical Device Design Engineers, Product Managers, Directors of Product Development, VP of Product Development, Inventors, Project Leaders, Technical Team Leaders
Webinar Includes:
Q/A Session with the Expert to ask your question
PDF print only copy of PowerPoint slides
60 Minutes Live Presentation
Certificate of Attendance
We will give you the steps and information to develop a medical device product. The documentation discussed can also be used and is often requested by the FDA and required by many ISO procedures for controlling the design process. We will discuss why certain steps are so important in the design process and that many steps are not just wasted time and paperwork. The process is a methodical approach that can be used with almost any product development process from concept to production. The speaker has a proven track record of successful products and many of them have been on the market longer than the 5 or 10 year expected product life cycle. The speaker has 20 granted patents and over 83% percent of them have been commercialized and using this process.
Why should you attend :
The medical device development process can be long and costly, but not if you follow some proven guidelines and steps. Sometimes projects are continuously pushed forward without doing proper reviews to see if the project warrants going to the next step. The sooner this process is done the better as it saves time and money. Good products also need to be completed faster and with less capital to beat the competition to market and beat them with a good quality product that needs little to no revisions and one that receives very few to no complaints from the customer. We will teach you the secrets of turning your medical device ideas into profit making products, which are the same steps that can also enable you to see why the project should be cancelled.
Areas Covered in the Session:
How to start a development project.
Patent search
Putting together a comprehensive systems requirement document.
1-10-100 Rule
Market research and customer needs
Design in quality & manufacturability
Prototype & testing
Production tooling
Qualification, Validation, & Verification
Trace matrix
Technical File & Regulatory Documentation
Who will benefit: (Titles)
Medical Device Design Engineers, Product Managers, Directors of Product Development, VP of Product Development, Inventors, Project Leaders, Technical Team Leaders
Webinar Includes:
Q/A Session with the Expert to ask your question
PDF print only copy of PowerPoint slides
60 Minutes Live Presentation
Certificate of Attendance
Other CFPs
- Implementing Adequate CAPA and Design Control Procedures
- 21 CFR Part 11 Add-On Inspections by the FDA
- Design Inputs - Design Outputs Traceability Matrix - Principles of Lean Documents and Lean Configuration
- International Conference on Advanced Materials, Mechanical Engineering and Technology (ICAMMET 2015)
- International Conference on Applied Mechanics, Materials and Structural Engineering (ICAMMSE 2015)
Last modified: 2014-10-17 14:35:01