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Lean Principles to Design Inputs, Design Outputs and Traceability Matrices

onlinecompliancepanel

Friday, June 16, 2017 from 11:30 AM to 2:30 PM (PDT)

Ticket Information

Ticket Type Remaining Sales End Price Fee Quantity
Live Session
for one participant
30 Tickets Jun 30, 2017 $250.00 $14.74
Super combo offer
Live Session for one Participant + Recorded Session
30 Tickets Jun 30, 2017 $500.00 $28.49
Special Offer
Live Session for one Participant + Training CD
30 Tickets Jun 30, 2017 $625.00 $35.37
Corporate Live Session
Unlimited Participants
30 Tickets Jun 30, 2017 $1,250.00 $57.45

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Description
Design controls involve the translation of user requirements (aka Voice of the Customer) into specific technical requirements as design inputs. These design inputs then form the basis of the design specification, which becomes the design output. Since design controls requires tracing backwards and forwards in order to link the requirements to their satisfaction, a problem faced by many companies is in having to maintain duplicate information across many controlled documents. This repetition is a major source of inconsistencies and errors. In this webinar, we apply the Theory of Lean documents and its corollary Theory of Lean Configuration to present a fresh approach to these linked and cascading documents.

Objectives of the Presentation
  • Brief introduction to lean documents and lean configuration
  • Quality System Regulation, 21 CFR Part 820 and ISO 13485 as these apply to design control documents
  • Traceability Matrix
  • Applying lean document and lean configuration principles to the above
  • Bringing it all together
Why Should you Attend
If you are constantly struggling to create, manage and maintain all of the information found in Design Inputs, Design Outputs and traceability matrices, all of which are often redundant, repetitive, and clustered together in an awkward manner, this webinar is something that will give you a different perspective and a very different approach that you can use.

If your design and manufacturing resources are spending too much time on documentation and not enough time on actual design and manufacturing you as a manager need to be looking for ways to simplify their work. This webinar presents a new approach based on solid principles and proven practices.

Who will Benefit
Managers, Supervisors, Directors, and Vice-Presidents in the areas of:
  • R&D
  • Manufacturing Engineering
  • Design Assurance
  • Quality Assurance
  • Operations
  • Document Control.
For Registration


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onlinecompliancepanel

Online Compliance Panel creates and delivers comprehensive industry relevant training sessions. These sessions are simple, interactive and cost effective. We are a predominantly web based information exchange forum. Live interactions on compliance training make the process holistic and effective. Online Compliance Panel largely emphasizes in offering regulatory compliance training to compliance professionals on varied topics. These primarily include risk management, quality management, corporate compliance and other regulatory compliances. Some of our primary areas of focus include advancement and updates in regulatory compliance, best practices and market trends.

We strive to incorporate high standards in developing a culture facilitating exchange of ideas resulting in functional excellence. Online Compliance Panel believes in nurturing ideas and thought processes through innovative e-learning methodologies. Our products and services are designed to offer customized solutions to industry and market. We bridge the gap between experience and knowledge thus delivering original and creative content.

Our objectives of employing interactive mediums ensure effective communication and mutual exchange of ideas. Online Compliance Panel closely follows best practices and regulatory trends in the global compliance scenario. We also observe and communicate trends witnessed in FDA, ISO regulations, process and design validation. All updates and additions to important laws can be accessed by our customers in real time.

Our mission is to empower compliance professionals through effective online training sessions. Our world class training methodologies stem from comprehensive understanding of client requirements. The content conforming to FDA and ISO standards is developed by well qualified and experienced industry leaders. Our offerings will exceed expectations and add value to your investment.

The content in various categories such as medical devices, pharmaceuticals and biotechnology will raise the bar in terms of quality already on offer .We hope to contribute to the creation of responsible organizations creating benchmarks in quality, integrity and transparency.

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Lean Principles to Design Inputs, Design Outputs and Traceability Matrices
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