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Register now to attend this premier event!


This third annual conference is designed to provide scientists and QA professionals with detailed information on pitfalls, challenges and solutions surrounding GLP procedures and to improve the outcomes of audits. The newest information on method qualification and validation, as well as the do’s and don’t’s for the GLP audit are being discussed by experts and case studies will be given. Good quality also depends on the first steps taken, it is extremely important to understand and draft good audit reports, as well as Standard Operating Procedures (SOP’s).

Pre-Conference
Workshop

Writing SOP’s 101:
An Introduction to GLP Standard Operating Procedures 
 
Dr. Alex D. Kanarek, President, Bio-Development Consulting Services

Conference
Session Topics


4 Method Qualification
4 Audits
4 Documentation and Data Management
4 Outsourcing and Multiple Studies

NEW THIS YEAR!
Roundtable
Discussions


Topic 1: FDA 483 Warning Letters
Topic 2: How to Audit Effectively
Topic 3: In House vs. Outsourcing

For more information, please contact:
Margit Eder, Ph.D., Conference Director, Cambridge Healthtech Institute
Phone: 781-972-5478 E-mail: meder@healthtech.com  

For exhibits and sponsorship information, please contact: 
David Karp at 781-972-5483 or dkarp@healthtech.com

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Cambridge Healthtech Institute  |  250 First Avenue  |  Suite 300   |   Needham,  MA  02494
Phone: 781-972-5400  |   Fax: 781-972-5425
chi@healthtech.com