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Webinar On Implementing Adequate CAPA and Design Control Procedures

  October 01, 2015  

Compliance Trainings, Mississauga

Description :

Device firms, who are intending to bring medical device products into the US market, are subject to quality system regulations.

Recent FDA enforcement trends (including 2013) reveal that both design control and Corrective and Preventive Action (CAPA) systems are critical elements to sustain FDA inspections.

Device manufacturers are required to establish and maintain FDA-compliant quality management systems, where appropriate and applicable, including design control and CAPA systems. This webinar is intended to provide guidance on understanding, interpreting, and implementing design control and CAPA system requirements.  This presentation is further intended to help you establish and maintain adequate design control and CAPA procedures for all classes of medical devices including IVDs.

Understanding, interpreting, and implementing design control and CAPA system requirements in a holistic manner can significantly contribute to your product quality and regulatory compliance, helping to ensure your innovative medical products to be safe and effective on a global market and saving enormous amount of your unnecessary time, efforts and investment.

This 60-min webinar will provide great opportunities for you to get familiar with regulatory and quality requirements for design control and CAPA systems applicable to all types of medical devices including IVDs.

This webinar is intended to help you learn and ensure you can implement adequate CAPA and design control procedures. In addition, this webinar will provide an opportunity to better understand and adequately implement adequate design control and CAPA systems.

Areas Covered in the Session :

Applicable Laws and Regulations

Statutory and Regulatory Requirements

Introduction and Definitions

Design and Development Planning

Design Input and Design Output

Design Review

Design Verification And Validation

Design Transfer and Design Changes

Design History File (DHF), Device History Record (DHR) and Device Master Record (DMR)

Corrective and Preventive Action (CAPA)

Root Cause Analysis

CAPA Elements

Common Problems

How to Avoid Common Mistakes

Speaker’s Recommendation and Suggestions on PASS-IT Solutions

Who Will Benefit:



Compliance Officers

Clinical Affairs (Associates, Specialists, Managers, Directors and VPs)

Regulatory Affairs (Associates, Specialists, Managers, Directors and VPs)

Quality Assurance (Associates, Specialists, Managers, Directors and VPs)

R&D (Engineers, Scientists, Managers, Directors and VPs)





Organized by: Compliance Trainings
Invited Speakers: Dr. David Lim, Ph.D., RAC, ASQ-CQA. Dr. Lim is President and Principal of Regulatory Doctor (www.RegulatoryDoctor.com). Dr. Lim frequently presents global regulatory and quality compliance topics in various forums and meetings. Recently, Dr. Lim developed 510(k) templates ready for use compliant with e-Copy and RTA policy. In addition, Dr. Lim developed FDA inspection checklists for drug and medical device manufacturers based on his analysis of FDA inspectional observations cited in 483s for the past seven years.
Deadline for Abstracts: 2015-10-22

For more information about this event please visit





To register this webinar 

E-mail: suzzane.d@compliancetrainings.com
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