Online Training 2015 - The Secrets of Successful Medical Development Process. - By Compliance Global Inc
Date2015-05-12
Deadline2015-05-12
VenueCompliance Global Inc. 2754 80th Avenue, New Hyde Park, NY 11040, USA - United States
KeywordsMedical equipment sales; Medical device development; Production planning tools
Topics/Call fo Papers
Overview:
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 design 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
? Requirements Traceability Matrix
? Technical File & Regulatory Compliance
Learning Objectives:
? The complete medical device product development process.
Who Will Benefit:
? Medical Device Design Engineers
? Product Managers
? Directors of Product Development
? VP’s of Product Development
? Inventors
? Project Leaders
? Technical Team Leaders
Level:
Intermediate
For more detail please click on this below link:
https://www.complianceglobal.us/product/700086
Email: referrals-AT-complianceglobal.us
Toll Free: +1-844-746-4244
Tel: +1-516-900-5515
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 design 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
? Requirements Traceability Matrix
? Technical File & Regulatory Compliance
Learning Objectives:
? The complete medical device product development process.
Who Will Benefit:
? Medical Device Design Engineers
? Product Managers
? Directors of Product Development
? VP’s of Product Development
? Inventors
? Project Leaders
? Technical Team Leaders
Level:
Intermediate
For more detail please click on this below link:
https://www.complianceglobal.us/product/700086
Email: referrals-AT-complianceglobal.us
Toll Free: +1-844-746-4244
Tel: +1-516-900-5515
Other CFPs
- Reviewing the processes to assess laboratory risks in terms of both Health and Safety. - By Compliance Global Inc
- Registration & Listing, FDA Inspection Strategies and Compliance Initiatives ? Medical Device. - By Compliance Global Inc
- Updating Your Employee Handbook: A 2015 Perspective. - By Compliance Global Inc
- Managing Through Chaos: Tools, Tips and Techniques to Set Priorities and Make Effective Decisions Under Pressure. - By Compliance Global Inc
- Proper Documentation to Avoid Costly Lawsuits - By Compliance Global Inc
Last modified: 2015-04-17 14:12:26