Pack of SEVEN: Best Selling Webinars by GlobalCompliancePanel

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Pack of SEVEN: Best Selling Webinars by GlobalCompliancePanel Powered By Docstoc

    Webinar Pack
    Pack of SEVEN: Best Selling Webinars by GlobalCompliancePanel
     Actual Price:        $2065.00

     Your Price:          $795.00
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    Understanding Attribute Acceptance Sampling
    including Z1.4 and c=0 Plans
    This course provides the attendees with the tools needed to
    understand and implement acceptance sampling.

    We explain the basis for sampling plans, the binomial distribution,
    and show how it helps us understand the sampling plan’s                                         Dan OLeary
    performance using the operating characteristic (OC) curve.                               President, Ombu Enterprises

    Statistical Concepts of Process Validation                                        Dan is the President of Ombu
    The FDA QSR requires device manufacturers to validate processes                   Enterprises, LLC, a company offering
                                                                                      training and execution in Operational
    when the manufacturer cannot "fully verify the output".
                                                                                      Excellence, focused on analytic skills
                                                                                      and a systems approach to
    The manufacturer must validate these processes with a "high                       operations management. ..more
    degree of assurance". The presentation explores the statistical
    underpinnings of these two phrases. To "fully verify the output"                                 Jeff Kasoff
    relates to the use of statistical sampling plans, while "high degree                        Director of Regulatory
    of precision" relates to process capability.                                                Affairs, Life-Tech, Inc

    The FDA Inspection Process: From SOP to 483                                       Jeff Kasoff, RAC, is the Director of
    Does the FDA call in advance or just show up at my door? Where do                 Quality at Byrne Medical, a leading
    I let the inspector go? Do I give them a tour? What should I let                  manufacturer of endoscopy
                                                                                      products. In this position, Jeff is
    them see? Who should I let them talk to? Are they ever going to
                                                                                      responsible for supplier
                                                                                      management. ..more

    Good Documentation Practices for GMP Operations                                               Kerry Paul Potter
    Whether you work in production or in a laboratory or if you conduct                           President, Summit
    investigations or finalize product release, sound data and                                     Consulting, Inc.
    information is essential to success and compliance. To ensure
    success and avoid those frustrating, embarrassing discussions of                  Kerry gained his pharmaceutical
    missing or doubtful data, laboratory employees must follow good                   manufacturing experience during his
    documentation practices.                                                          28-year career with Merck. His
                                                                                      career spanned the areas of Quality
                                                                                      Operations, Audits & Inspections,
    21 CFR Part 11 - Compliance for Electronic Records                                Laboratory. ..more
    and Signatures
    This webinar details the regulation and how it applies to
                                                                                                  David Nettleton
    computerized systems.
                                                                                              FDA Compliance Specialist,

    Learn exactly what is needed to be compliant for all three primary
                                                                                      David Nettleton, is an FDA
    areas: SOPs for the IT infrastructure, industry standards for
                                                                                      Compliance Specialist for 21 CFR
    software product features, and the 10-step risk-based validation
                                                                                      Part 11, HIPAA, and Computer
    approach.                                                                         System Validation. His latest book is
                                                                                      "Risk Based Software Validation -
    Excel Spreadsheets and FDA Device Regulations                                     Ten easy Steps". ..more
    This webinar helps you understand the FDA device regulations
    related to Excel spreadsheets.                                                                    Jose Mora
                                                                                              Principal Consultant, Atzari
    These spreadsheets can be automated processes and create                                        Consulting, LLC

    electronic records.
                                                                                      José Mora is a Principal Consultant
                                                                                      specializing in Manufacturing
    Design Inputs - Design Outputs Traceability Matrix -                              Engineering and Quality Systems.
    Principles of Lean Documents and Lean Configuration                               For over 29 years he has worked in
    Design Inputs, Design Outputs, and Traceability matrices present a                the medical device industry
    challenge to almost all industries that apply design controls.                    specializing in manufacturing,
                                                                                      process development, tooling, and
    Typically, these cause the creation and maintenance of duplicate                  quality systems. ..more
    information across various documents - a major source of errors.

    Click here to buy the webinar pack
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    It would be really nice if you can circulate this mail to all your deserving colleagues who can immensely
    benefit from this program.

    For more information, please contact the event coordinator. We look forward to seeing you at the webinar.

    Best regards,
About GlobalCompliancePanel
GlobalCompliancePanel is an online knowledge fulfillment community portal & it has put together a new model for online
compliance training by creating a single window of learning opportunities for compliance professionals & providing a
forum for expert speakers/panelists to render their services through simplified online training delivery mechanisms. Our
commitment is give compliance regulatory training, showcasing of best industry practices & quality enrichment training
sessions in a most cost effective manner. Compliance professionals can benefit from a wide range of training sessions,
giving a diverse choice of events & all sessions being either Live or recorded stream or in the form of audio CDs.
GlobalCompliancePanel portal ensures a secure & cost effective online environment and also support your E-learning
and development on/through our website. Keep track of all webinars arranged for your industry through notifications &
event calendars being mailed to your inbox. GlobalCompliancePanel opens new doors of learning opportunities for

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Description: This course provides the attendees with the tools needed to understand and implement acceptance sampling. We explain the basis for sampling plans, the binomial distribution, and show how it helps us understand the sampling plan’s performance using the operating characteristic (OC) curve