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Compliance Training Panel.

Compliance Training Panel provides Quality trainings through their world class platform which enables the clients to discuss with industry experts and to gain related information.

Compliance Training Panel has been established by professionals in the field of Quality, Compliance Auditing and Health Care, Education & Finance with an objective to create an ecosystem that will deliver quality training's on compliance of various regulatory and legal requirements.

We are a US based organization specializing in online trainings in the form of Webinars and Seminars.


Effective Design of Experiments (DOE) Strategies
Description :
The effective and progressive use of a Screening DOE, a Mapping DOE and a Robust Process DOE will lead to a better understanding of the process and the location of the best optimum. NOTE: This webinar focuses on DOE strategies. It is not focused on statistical methods, analysis of variance, and other techniques, but rather the overall approach for successful DOEs.
Why ?
  • Effective DOE strategies
  • Avoiding pitfalls when performing DOEs
  • How to capture the essence of a process
  • Using the right resolution at the right time
  • Use of DOEs during process validation
  • How to prevent "expert" bias when designing experiments
  • Letting the process do the talking
  • "Poke the Alligator" - see how the process reacts
  • Areas Covered in the Session :
    1. Gauge R&R considerations
    2. Screening DOEs
    3. Mapping DOEs
    4. Robust Process DOEs
    5. Use of Six Sigma DMAIC when using DOEs and vice versa
    6. Obtaining proper input from various stakeholders
    7. Use of DOEs during process validation
    Who Will Benefit:
    Managers, Supervisors, Directors, and Vice-Presidents in the areas of:
    • R&D
    • Manufacturing Engineering
    • Quality Assurance
    About Speaker:
    José Mora is a Principal Consultant and Project Manager specializing in Manufacturing Engineering, Quality Systems, and Lean Transformations. José is a recognized subject matter expert in process validation, lean manufacturing, lean controlled document systems, startup operations, process development and quality systems, having lectured internationally and presented webinars on these subjects.For over 30 years he has worked in the life sciences in positions ranging from Senior Engineer and Project Manager to Vice-President, specializing in manufacturing, process development, tooling, and quality systems. His medical device experience includes surgical instruments, PTA & PTCA dilatation and guiding catheters, plastic surgery implants and tissue expanders, urology implants and devices for the treatment of incontinence, delivery systems for brachytherapy, orthopaedic implants and instruments, and vascular surgery grafts and textiles.

    Wherever he has worked, Jose has a track record of introducing world-class methodologies such as Kepner-Tregoe, Taguchi techniques, Theory of Constraints, Lean Manufacturing, Five S (Visual Workplace), process validation to Global Harmonization Task Force standards, and similar approaches. He has implemented various good manufacturing practices like JIT, kanban systems, visual workplace and lean manufacturing practices. Jose has also published a white paper on the application of lean manufacturing methods to the creation and management of controlled documents and a template for strategic deployment.
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