Events



You Are Here: Event > Excusive (No Cost) FEA/CFD Simulation Seminar for Designers/CAD Users

Excusive (No Cost) FEA/CFD Simulation Seminar for Designers/CAD Users


Thursday, 15th August 2013 To Saturday, 15th August 2009
09.00 AM 
 
2930 S Sheridan Way
Oakville Ontario L6J 7J8



Report Abuse

re you a Designer/Drafting Professional/CAD User/Technologist? Are you little hesitant to do Design Validation/Simulation? and do you often ask yourself these questions :
•Will I be able to do simulation to test designs without prior experience?
•Will I be able to run the simulation/design validation/analysis correctly?
•Concerned about design validation results accuracy?

FEA Training Consultants Inc. a Simulation Powerhouse based in Mississauga,ON cordially invites you to this one of a kind exclusive Simulation (FEA/CFD) Training Seminar. This seminar is presented by FEA's Expert Team of over 40 years of combined experience in educating CAD Users, Designers and Drafting Professionals to perform design validation efficiently.

AGENDA:
Learn how Product Designers/CAD Users/Drafting Professionals/Technologists use SolidWorks Simulation to:
•Perform virtual load testing, determine deflection and Safety factor check.
•Reduce costs, eliminate time consuming prototyping cycles and improve your product performance with design optimization and fatigue testing.
•Optimize your designs for internal or external flow conditions.
•Solve your computational flow challenges with CFD.
•Avoid overheating of components.
•Improve your Product Quality.
FEA Training Consultants Inc.
Phone: 9059900094
Report Abuse
 
Want to manage/update/remove your Listings?
Please enter your email or user-id
List your Event

Similar Events

Mississauga: Web Design In Mississauga (6472944444)
======================================================================================= Web Design In Mississauga (6472944444) Web Design Canada Mississauga http://logoman.ca/ Canada -Ontario -Mississauga Web Design Compan
Date Posted: 06-Oct-14


FL: Live Webinar Design Control Under 21 CFR 820 (the CGMPs) and ISO 13485
Live Webinar Design Control Under 21 CFR 820 (the CGMPs) and ISO 13485 Description The FDA CGMPs (21 CFR 820.30) and ISO QMS’ (ISO 13485:2016 7.3) expect companies to perform meaningful, results driven Design Control act
Date Posted: 27-Apr-18


Houston: Hypothesis Testing for Means ? A Practical Approach
DESCRIPTION One common statistical technique, especially useful in quality engineering and manufacturing, is the hypothesis test. While it is common, it can be confusing and not well understood. In addition, some instances can involve complicated
Date Posted: 18-Apr-16


NORTH YORK: SAP HR STANDARD CLASS!!!!!!!!!
SAP HR STANDARD CLASS!!!!!!!!! - Thursday, Oct.4th, 2007 -----7:30—9:30pm - Friday, Oct.5th, 2007 ---- 7:30—9:30pm Why you should NOT miss this seminar? Currently, the SAP marketing in North America is dramatically growing. According the
Date Posted: 29-Sep-07


FL: Live Webinar Understanding and Implementing a Quality by Design Progra
Description This training will explain the main principles behind a QbD approach and provide guidelines in how to implement the concepts into a pharmaceutical development organization. Topics covered will include the target product quality profile,
Date Posted: 26-Apr-18


FL: Live Webinar Understanding and Implementing a Quality by Design Progra
Description This training will explain the main principles behind a QbD approach and provide guidelines in how to implement the concepts into a pharmaceutical development organization. Topics covered will include the target product quality profile,
Date Posted: 26-Apr-18


FL: Live Webinar Construct and Manage the Technical File and Design Dossie
Live Webinar Construct and Manage the Technical File and Design Dossier Description This Webinar will provide a substantive overview and outline differences between the Technical File and Design Dossier for those device firms dealing with the glo
Date Posted: 30-Apr-18


FL: Live Webinar Understanding and Implementing a Quality by Design Progra
Description This training will explain the main principles behind a QbD approach and provide guidelines in how to implement the concepts into a pharmaceutical development organization. Topics covered will include the target product quality profile,
Date Posted: 26-Apr-18


Houston: Live Webinar :DHF, DMR, DHR, Technical File and Design Dossier - Key R
DESCRIPTION This webinar will examine the existing and proposed requirements for the FDA's DHF - including its derivative documents, the DMR and DHR. It will consider the MDD's TF/DD requirements, and evaluate the documents' differing purposes / g
Date Posted: 27-Apr-16


north york: Best SAP BO Class in Toronto! -SAP Training, Free Seminar
Best SAP BO Class in Toronto! - New Class Starts October 10 SAP BO (Business Objects®) Standard Class Starts October Free Seminar: Saturday, October 10, 2009, 10:00am Course Highlights: 1. Best Practice System: fully integrated with SAP BI
Date Posted: 09-Oct-09


Houston: Auditing the Risk Management File - By Dan O Leary
DESCRIPTION Medical device manufacturers must implement risk management systems for their devices. This can be a complicated system requiring a lot of work and multiple resources. If it is not correct, the regulatory authorities may require correc
Date Posted: 02-Feb-16


FL: Live Webinar Use / Human Factors Engineering to Satisfy the New IEC 62
Live Webinar Use / Human Factors Engineering to Satisfy the New IEC 62366-1, -2 Description IEC has released a new medical device usability standard, IEC 62366-1:2015 -- Part 1: “Application of the new Usability Engineering Standard to Medic
Date Posted: 30-Apr-18


Houston: Introduction to Risk Management: Medical Devices
DESCRIPTION This webinar will cover Risk Management per ISO 14971 throughout the product lifecycle. Risk Management is an important process to methodically and effectively identifying and mitigating risks in the product design and manufacturing p
Date Posted: 18-Apr-16


NEW JERSEY: 2 Day Workshop: Human Error: Why Human Error is the biggest downtime
2 Day Workshop: Human Error: Why Human Error is the biggest downtime problem in the manufacturing sector and how to investigate, control, reduce, and prevent to improve results. Location 1: New Brunswick May 10 - 11 Description Small mi
Date Posted: 04-May-18


north york: SAP HR SEMINAR, FREE!!!!!!!!!
SAP HR SEMINAR, FREE!!!!!!!!! - Sunday, Sep Why you should NOT miss this seminar?  Currently, the SAP marketing in North America is dramatically growing. According the statistic, over 10,400 SAP positions are available in
Date Posted: 22-Sep-07


Map locations are shown as per geocoding services and they depeneds on the accuracy of the address. If address is wrong it may show wrong map. If you put a listing which shows wrong map, please remove the listing and create a new one with correct address details.

Please note: The information on this site is submitted by users. CanadianDesi never checks accuracy of the information. Please use this information at your risk. If you have any question or concern regarding this listing, or you know that the above information is not accurate, please Contact Us. Thanks.
Please note: The information on this site is submitted by users. CanadianDesi never checks accuracy of the information. Please use this information at your risk. If you have any question or concern regarding this listing, or you know that the above information is not accurate, please Contact Us. Thanks. 


Share:
















Advertise Contact Us Privacy Policy and Terms of Usage FAQ
Canadian Desi
© 2001 Marg eSolutions


Site designed, developed and maintained by Marg eSolutions Inc.