2-day In-person Seminar 2015 - 2-day In-person Seminar on Using Statistical Methods for ICH Guidelines at Zurich, Switzerland

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 facts 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
o Regression - Q1
o Design of Experiments and ANOVA - Q8
o Sample Size - Q6
o Probability - Q9
o Interactive Discussion/Questions
? Developing a risk strategy
Who Will Benefit:
? Quality Managers
? Assay Development Scientists
? Quality Analysts
? Research Scientists
? Risk Managers
? Quality Managers
Agenda
Day One:
Lecture 1: Introduction/Fundamentals - Statistics
? Summary Statistics
? Graphical Techniques
? Hypothesis Testing
? Confidence Intervals and Tolerance Intervals
? Interactive Discussion/Questions
Lecture 2: ICH "Q" Series
? Q1 Stability Testing
? Q2 Validation of Analytical Procedures
? Q3 Impurities in New Drug Substances
? Q5 Viral Safety Evaluation of Biotechnology Products Derived from Cell Lines of Human of Animal Origin
? Q6 Specifications
? Q7 GMP for API
? Q8 Pharmaceutical Development
? Q9 Quality Risk Management
? Q10 Pharmaceutical Quality System
Day Two:
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
Instructor Profile:
Steven Walfish
President, Statistical Outsourcing Services
Mr. Walfish is a Principal Statistician at BD in Franklin Lakes, NJ. He is responsible for supporting continuous improvement efforts and process development for worldwide operations. Prior to BD he was a statistician at GE Healthcare in Waukesha, WI. Previously, Steven was President of Statistical Outsourcing Services, a consulting company that provides statistical analysis and training to the FDA regulated industries. Prior to starting Statistical Outsourcing Services, Mr. Walfish was the Senior Manager Biostatistics, Non-clinical at Human Genome Sciences in Rockville MD. Mr. Walfish brings over 20 years of industrial expertise in the development and application of statistical methods for solving complex business issues including data collection, analysis and reporting. Steven has experience applying statistical methods to design control verification and validation. Steven has been part of three 510(k) submission and numerous meetings with the FDA.
Location: Zurich, Switzerland Date: September 3rd & 4th, 2015 Time: 9 AM to 6 PM
Venue: Hilton Zurich Airport
Venue Address: Hohenbuhlstrasse 10, 8152 Opfikon-Glattbrugg, Switzerland.
Price: $1,595.00 (Seminar for One Delegate)
Register now and save $200. (Early Bird)
Until July 10, Early Bird Price: $1,595.00
From July 11 to September 01, Regular Price: $1,795.00
Registration Details:
NetZealous LLC,
DBA GlobalCompliancePanel
161 Mission Falls Lane,
Suite 216, Fremont, CA 94539, USA
USA Phone: 1-800-447-9407
Fax: 302-288-6884
support-AT-globalcompliancepanel.com
http://www.globalcompliancepanel.com
Registration Link - http://bit.ly/1IMw5SS