|
TELECONFERENCE DESCRIPTION |
|
Manufacturers design and develop products based on an expected
product lifetime. Many manufacturers conduct extensive
reliability testing to minimize the risk that products will fail
prematurely. Despite these efforts, unexpected failures occur
due to design flaws, manufacturing process changes, or a
misunderstanding of the product use environment.
Premature
failures alienate customers and significantly impair brand and
company reputations. Failure data may be easily modeled to
forecast future failures and identify emerging issues that
present financial risks to the organization.
This 60-minute presentation will show how you can use failure
data to predict expected future failures, proactively drive
quality and reliability improvement and react quickly to
emerging issues.
|
| AREAS
COVERED IN THE SEMINAR |
-
Modeling Time-To-Failure Data.
-
Predicting Future Failures.
-
Developing a Warranty Forecast.
-
Accounting for Model Uncertainty.
-
Identifying Non-Homogeneous Groups.
-
Handling Non-Homogenous Groups (e.g. Model
Revisions / Design Levels).
|
|
WHO WILL BENEFIT |
-
Product Development Personnel
-
Product Engineers
-
Managers
-
Executives Finance Staff Reliability
Professionals Quality Personnel
|
|
INSTRUCTOR PROFILE |
|
Steven Wachs, has
25 years of wide-ranging industry experience in both technical
and management positions. Steve has worked as a statistician at
Ford Motor Company where he has extensive experience in the
development of statistical models, reliability analysis,
designed experimentation, and statistical process control.
Steve is currently a Principal Statistician at Integral
Concepts, Inc. where he assists manufacturers in the application
of statistical methods to reduce variation and improve quality
and productivity. He also possesses expertise in the application
of reliability methods to achieve robust and reliable products
as well as to estimate and reduce warranty. In addition to
providing consulting services, Steve regularly conducts
workshops in industrial statistical methods for companies
worldwide.
|
| REGISTER |
|
Registration - Session Only: $199.00
CD Recording Only: $449.00
|
|
Upcoming Teleconferences
Audit/Inspection Preparedness for Clinical
Research/Site Coordinators
March 6, 2012
Registration - Session Only: $249.00
CD Recording Only: $449.00
Learn More
3-hr Virtual Seminar - Medical Device Adverse
Event Reporting and
Vigilance System During Clinical Trials and Post-Marketing: US, EU,
and Canada
March 6, 2012
Registration - Session Only: $449.00
CD Recording Only: $799.00
Learn More
Software Verification and Validation Planning
and Implementation
March 6, 2012
Registration - Session Only: $299.00
CD Recording Only: $599.00
Learn More
Social Media in a Regulated Environment (for
Financial Services)
March 7, 2012
Registration - Session Only: $199.00
CD Recording Only: $399.00
Learn More
Webinar: When Do You Need a 510k?
March 7, 2012
Registration - Session Only: $249.00
CD Recording Only: $449.00
Learn More
Method Validation in Drug Development Process -
Common Mistakes
and Issues
March 7, 2012
Registration - Session Only: $249.00
CD Recording Only: $449.00
Learn More
Managing Immunogenicity Risk in
Biopharmaceuticals
March 8, 2012
Registration - Session Only: $249.00
CD Recording Only: $499.00
Learn More
FDA's Rules for Financial Disclosure in
Clinical Trials Clarified: New
Guidance, Practical Application
March 9, 2012
Registration - Session Only: $249.00
CD Recording Only: $449.00
Learn More
Reduce the Risks of Foreign Material
Contamination - A Manufacturer's
Guide in Creating a Foreign Material Control
March 12, 2012
Registration - Session Only: $199.00
CD Recording Only: $449.00
Learn More
Validation of Bioanalytical Methods and
Procedures for FDA Compliance
March 14, 2012
Registration - Session Only: $299.00
CD Recording Only: $499.00
Learn More
Ethical Hotlines, Whistleblowers and Compliance
with the EU Data Privacy Laws & Regulations
March 15, 2012
Registration - Session Only: $199.00
CD Recording Only: $449.00
Learn More
Setting up an Effective Risk Management Program
March 16, 2012
Registration - Session Only: $199.00
CD Recording Only: $449.00
Learn More
Understanding Disinfection and Cleanroom
Cleaning in an FDA Regulated Environment
March 16, 2012
Registration - Session Only: $299.00
CD Recording Only: $499.00
Learn More
Letter of Credit Terms and Conditions
March 16, 2012
Registration - Session Only: $199.00
CD Recording Only: $449.00
Learn More
Doing Business Despite Embargoes and Sanctions:
OFAC Licensing
March 16, 2012
Registration - Session Only: $199.00
CD Recording Only: $399.00
Learn More
Full Day Virtual Seminar - US, EU and Japan GMP
Requirements:
Practical ICH Area Differences, Healthcare Authority Inspection
Focus
March 16, 2012
Registration - Session Only: $549.00
CD Recording Only: $999.00
Learn More
OSHA Inspections - Avoiding the 10 Most Common
Mistakes
March 19, 2012
Registration - Session Only: $199.00
CD Recording Only: $449.00
Learn More
How to Survive a DEA Audit
March 20, 2012
Registration - Session Only: $449.00
CD Recording Only: $649.00
Learn More
How to Establish an Effective Good Clinical
Practice in Drugs and
Medical Devices
March 20, 2012
Registration - Session Only: $249.00
CD Recording Only: $399.00
Learn More
Project Management to Meet CGMP Requirements
March 20, 2012
Registration - Session Only: $299.00
CD Recording Only: $499.00
Learn More
Water System Mythology: Common False Beliefs
for Microbial Control and Monitoring
March 21, 2012
Registration - Session Only: $249.00
CD Recording Only: $499.00
Learn More
Implementation of Pharmacogenomics into the
Routine Clinical Laboratory
March 21, 2012
Registration - Session Only: $299.00
CD Recording Only: $499.00
Learn More
Best Practices for Maintaining an IND and IDE
Application with the FDA
March 21, 2012
Registration - Session Only: $249.00
CD Recording Only: $449.00
Learn More
Foreign Corrupt Practices Act (FCPA) Webinar
March 21, 2012
Registration - Session Only: $149.00
CD Recording Only: $299.00
Learn More
Archiving GLP Records: How Archiving Makes or
Breaks the Audit
March 22, 2012
Registration - Session Only: $249.00
CD Recording Only: $499.00
Learn More
Medical Device Risk Management Using ISO 14971
March 23, 2012
Registration - Session Only: $299.00
CD Recording Only: $549.00
Learn More
Elegant Quality Assurance Practices for Device
Efficacy and Efficiency
Requirements
March 23, 2012
Registration - Session Only: $299.00
CD Recording Only: $549.00
Learn More
Environmental Monitoring and Contamination
Control Plan
March 27, 2012
Registration - Session Only: $299.00
CD Recording Only: $499.00
Learn More
Laboratory Investigations for Out of
Specification Results
March 28, 2012
Registration - Session Only: $299.00
CD Recording Only: $499.00
Learn More
Foreign Manufacturing Facilities - Avoiding
Problems with FDA
March 29, 2012
Registration - Session Only: $299.00
CD Recording Only: $549.00
Learn More
INCOTERMS - International Commercial Terms
March 30, 2012
Registration - Session Only: $199.00
CD Recording Only: $449.00
Learn More
Full-day Virtual Seminar - Quality Agreements
with Pharmaceutical/
Biologic Manufacturers and the Use of Drug Master Files:
Understanding and
Meeting Your Regulatory and Processing Responsibilities
March 30, 2012
Registration - Session Only: $749.00
CD Recording Only: $1,099.00
Learn More
|
