2015 - Webinar On Preventing Medical Device Recalls
Date2015-10-26
Deadline2015-10-26
VenueOnline, Canada
KeywordsMedical device webinar; Medical Device Compliance; Medical Device Recalls
Topics/Call fo Papers
The webinar will provide an overview and a foundation for further learning concerning preventing recalls during specification writing, risk assessment and risk management, preventing recalls during the early design and the detail design phases of development, and preventing recalls during validation, verification, and software design.
Areas Covered in the Session :
Preventing recalls during specification writing
Preventing recalls during early design
Preventing recalls during the detail design phase
Designing for Prognostics to protect patients
Preventing recalls during production validation
Preventing software design recalls
Preventing supply chain quality defects to avoid recalls
Preventing recalls using a verification process
Preventing recalls using the design validation process
Role of management in preventing recalls
Innovative methods useful in preventing recalls
Who Will Benefit:
Quality Professionals
Regulatory Professionals
Manufacturing & Design Engineers
Compliance Departments
Research & Development Teams
Documentation Personnel
Complaint Handling Personnel
Product Development Teams
Areas Covered in the Session :
Preventing recalls during specification writing
Preventing recalls during early design
Preventing recalls during the detail design phase
Designing for Prognostics to protect patients
Preventing recalls during production validation
Preventing software design recalls
Preventing supply chain quality defects to avoid recalls
Preventing recalls using a verification process
Preventing recalls using the design validation process
Role of management in preventing recalls
Innovative methods useful in preventing recalls
Who Will Benefit:
Quality Professionals
Regulatory Professionals
Manufacturing & Design Engineers
Compliance Departments
Research & Development Teams
Documentation Personnel
Complaint Handling Personnel
Product Development Teams
Other CFPs
- Webinar On Preparing for FDA BIMO Inspection and Management
- Webinar On In-House or Out-House (Contract Lab vs In-House Lab) - How to Overcome the Corporate Dilemma
- Webinar On Transferring Medical Device Production to a Contract Manufacturer - Decision Making Process and Procedures
- Webinar On Computer System Validation: Step-by-Step
- Webinar On Understanding the FDA’s Quality System Regulation, 21 CFR, Part 820
Last modified: 2015-09-29 20:20:29