Sign for Notice Everyday    Sign Up| Sign In| Link| English|

Our Sponsors

    Receive Latest News

    Feedburner
    Share Us


    How can companies allocate scarce resources

    View: 219

    Website http://www.compliance4all.com/control/w_product/~product_id=501938LIVE?channel=ourglocal_Jun_2018_SE | Want to Edit it Edit Freely

    Category CAPA, FDA Expectations, Root Cause Analysis, Dietary Supplements, corrective action and preventive action, Compliance regulations, failure investigation, Conference on CAPA

    Deadline: June 24, 2018 | Date: June 27, 2018

    Venue/Country: Online, U.S.A

    Updated: 2018-04-18 15:38:08 (GMT+9)

    Call For Papers - CFP

    Overview:

    This webinar will help you understand the critical ingredients for conducting an effective root cause analysis, also you will learn how to Analyze and document the root cause of the problem.

    Why should you Attend:

    The billions of dollars spent by industry annually on quality / GMP are not providing the product safety or efficacy seemingly promised. And for most companies, the fixes are not rocket-science, but proper up-front risk-based, closed-loop failure investigation / root cause analysis as an integral part of CAPA, Validation and Quality Management Systems / cGMP planning, implementation and execution.

    Areas Covered in the Session:

    Regulatory "Hot Buttons"

    The 4 Basic Steps to Problem Solving

    A Suggested Investigation Template

    Monitor for Effectiveness

    Lock In the Change - Close the Loop

    Take It to the Next Level

    Who Will Benefit:

    Engineering

    Production

    Operations

    Consultants,Others Tasked with Product

    Speaker Profile:

    John E. Lincoln is a medical device and regulatory affairs consultant. He has helped companies to implement or modify their GMP systems and procedures, product risk management, U.S. FDA responses. In addition, he has successfully designed, written and run all types of process, equipment and software qualifications/validations, which have passed FDA audit or submission scrutiny, and described in peer-reviewed technical articles, and workshops, world wide.

    Event Fee: One Dial-in One Attendee Price: US$150.00

    Contact Detail:

    Compliance4All DBA NetZealous,

    Phone: +1-800-447-9407

    Email: supportatcompliance4All.com


    Keywords: Accepted papers list. Acceptance Rate. EI Compendex. Engineering Index. ISTP index. ISI index. Impact Factor.
    Disclaimer: ourGlocal is an open academical resource system, which anyone can edit or update. Usually, journal information updated by us, journal managers or others. So the information is old or wrong now. Specially, impact factor is changing every year. Even it was correct when updated, it may have been changed now. So please go to Thomson Reuters to confirm latest value about Journal impact factor.