Design Inputs Design Outputs Traceability Matrix - 2017

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Category manufacturing engineering and technology, engineering design process, fda spreadsheetvalidation guidance, usp 1029 good documentation practices, finance and management, quality control, quality assurance program, quality assurance plan

Deadline: April 11, 2017 | Date: April 12, 2017

Venue/Country: Fremont, U.S.A

Updated: 2017-02-24 18:52:36 (GMT+9)

Call For Papers - CFP

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.

Areas Covered in the Session:

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

Who Will Benefit:

Managers, Supervisors, Directors, and Vice-Presidents

R&D

Manufacturing Engineering

Design Assurance

Quality Assurance

Operations

Document Control

Speaker Profile:

Jose Mora is a Principal Consultant specializing in Manufacturing Engineering and Quality Systems. For over 30 years he has worked in the medical device industry specializing in manufacturing, process development, tooling, and quality systems. Prior to working full time as a consulting partner for Atzari Consulting, José served as Director of Manufacturing Engineering at Boston Scientific and as Quality Systems Manager at Stryker Orthopedics, where he introduced process performance, problem solving, and quality system methodologies.

Contact Detail:

Compliance4All DBA NetZealous,

Phone: +1-800-447-9407

Email: supportcompliance4All.com