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    2-day In-person seminar on Using Statistical Methods for ICH Guidelines at Boston, MA

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    Website http://bit.ly/Klaxl7 | Want to Edit it Edit Freely

    Category Seminar, Health, Medical, Pharma, Clinical

    Deadline: April 03, 2014 | Date: April 04, 2014-April 05, 2014

    Venue/Country: boston, U.S.A

    Updated: 2014-03-04 16:11:23 (GMT+9)

    Call For Papers - CFP

    Overview:

    This hands-on course will provide attendees with an understanding of how to apply statistical methods to the ICH Q series guidelines. The course will deliver tools, templates and insight that will allow participants to immediately begin implementation within their organization/firm.

    This 2 day hands-on workshop explores the unique challenges facing all facets of a pharmaceutical or biotechnology company. Practical implementation solutions as well as best practice descriptions that will allow management to effectively assess manage and mitigate risk of poorly designed studies. Participants will learn the major aspects of the statistical methods and discover how organizations and external authorities expect organizations to meet these guidelines.

    Areas Covered in the Session:

    Introduction to ICH Q Series

    Introduction/Fundamentals - Statistics

    Integrating Statistics into protocols

    Developing a risk strategy

    Course Outline:

    Day 1 ? Agenda

    Lecture 1: Introduction/Fundamentals - Statistics

    Summary Statistics

    Graphical Techniques

    Hypothesis Testing

    Confidence Intervals and Tolerance Intervals

    Lecture 2: ICH "Q" Series

    Q1 Stability Testing

    Q2 Validation of Analytical Procedures

    Q3 Impurities in New Drug Substances

    Q4 Pharmaceutical Development

    Q5 Quality Risk Management

    Q6 Pharmaceutical Quality System

    Day 2 ? Agenda

    Lecture 3: Integrating Statistics

    Regression - Q1

    Design of Experiments and ANOVA - Q8

    Sample Size - Q6

    Probability - Q9

    Interactive Discussion/Questions

    Lecture 4: Statistical Tools in Action

    Developing a Risk Management Plan

    Assay Validation

    Lecture 5: Setting Specifications

    Who Will Benefit:

    Quality Managers

    Assay Development Scientists

    Quality Analysts

    Research Scientists

    Risk Managers

    Quality Managers

    ABOUT SPEAKER ?

    Mr. Steven Walfish brings is the founder and President of Statistical Outsourcing Services. He brings nearly 20 years of industrial experience providing statistical solutions to complex business problems. Mr. Walfish was Senior Manager Biostatistics, Nonclinical at Human Genome Sciences in Rockville MD. Mr. Walfish has held positions with PricewaterhouseCoopers, Chiron Diagnostics and Johnson & Johnson. Mr. Walfish holds a Bachelors of Arts in Statistics from the University of Buffalo, Masters of Science in Statistics from Rutgers University and an Executive MBA from Boston University.

    Location: Boston, MA| 3rd & 4th April 2014 |9:00AM-6:00PM EDT

    Venue: Courtyard Boston Logan Airport

    Address: 225 William F. McClellan Highway - Boston, Massachusetts 02128 USA

    Price: $1,295.00

    Discount:

    Register now and save $200. (Early Bird)

    Until March 10, Early Bird Price: $1,295.00

    from March 11 to April 01, Regular Price: $1,495.00

    Contact Information:

    Event Coordinator

    Toll free: 1800 447 9407

    Fax: 302-288-6884

    Email: supportatglobalcompliancepanel.com

    Website: https://www.globalcompliancepanel.com

    LIVE CHAT SUPPORT - http://www.globalcompliancepanel.com/chat/client.php

    Event Link: http://bit.ly/Klaxl7

    GlobalCompliancePanel,

    161 Mission Falls Lane,

    Suite 216, Fremont, CA 94539, USA


    Keywords: Accepted papers list. Acceptance Rate. EI Compendex. Engineering Index. ISTP index. ISI index. Impact Factor.
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