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Two Day Course: Quality by Design - Essential Techniques for Medical Devices - ResearchAndMarkets.com

June 14, 2018

DUBLIN--(BUSINESS WIRE)--Jun 14, 2018--The “Quality by Design - Essential Techniques for Medical Devices” conference has been added to ResearchAndMarkets.com’s offering.

Course “Quality by Design - Essential Techniques for Medical Devices” has been pre-approved by RAPS as eligible for up to 12 credits towards a participant’s RAC recertification upon full completion.

Design Controls are essential for producing safe and effective medical devices. And Design Controls are considered a critical process by the FDA. Yet, Design Controls are still one of the most frequent areas for 483 and Warning Letter observations. This 2 day seminar will help you understand, develop, and implement design controls processes and tools that are a competitive strength for your company. You will learn how to incorporate design controls into your product development process to help streamline development and ensure quality and compliance.

In this seminar, we will cover Design Controls for medical devices. We will understand the requirements for design controls and how to translate them into an efficient and effective process for your company. We’ll cover the history, context, and requirements for design controls. Then we’ll discuss requirements and tools in detail and include exercises to help you practice and improve your design control process.

Why should you Attend:

The intrinsic quality, safety, and effectiveness of medical device are established during the design phase. Yet, statistics show that a significant percentage of all medical device recalls are due to design problems. And those design problems can have disastrous results for your customer and for your company. A rigorous and efficient design control process can help avoid these quality and compliance problems. Issues that are identified early are more easily and quickly resolved. This seminar will help you avoid design problems and their impact on quality, cost, speed to market, and customer satisfaction.

Design Control is one of the critical areas covered by the FDA in inspections of Medical Device Companies. Design issues can also result in complaints from your customers and in medical device reports. Design issues can even create issues with manufacturability for your company including low yields and excessive scrap and rework. Finding and fixing issues early on in design provide much more leverage than trying to fix problems for products already in production. This webinar can help you learn from past issues and improve your next generations of product.

Learning Objectives:

Using interactive discussion and exercises, students will understand the regulations, context, and history of design controls. They will learn how to use design control as a tool to ensure product quality while meeting business needs for speed to market.

They will come away with key concepts, practice in these concepts, and extensive course notes for future use and reference:

Expectations Regulations and History Design Control process, procedures, forms, records, files Linkages to the rest of your Quality Management System Lessons Learned Myths Challenges Best Practices Inspection Readiness

For more information about this conference visit https://www.researchandmarkets.com/research/rdcfbb/two_day_course?w=4

View source version on businesswire.com:https://www.businesswire.com/news/home/20180614006266/en/

CONTACT: ResearchAndMarkets.com

Laura Wood, Senior Manager

press@researchandmarkets.com

For E.S.T. Office Hours Call 1-917-300-0470

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Related Topics:Biotechnology,Medical Devices,Pharmaceutical Manufacturing

KEYWORD:

INDUSTRY KEYWORD: HEALTH MEDICAL DEVICES

SOURCE: Research and Markets

Copyright Business Wire 2018.

PUB: 06/14/2018 05:14 PM/DISC: 06/14/2018 05:14 PM

http://www.businesswire.com/news/home/20180614006266/en

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