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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).
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Writing SOP’s 101:
An Introduction to GLP Standard Operating Procedures
Dr. Alex D. Kanarek, President, Bio-Development
Consulting Services
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Conference
Session Topics |
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4
Method
Qualification
4 Audits
4 Documentation and Data Management
4 Outsourcing and Multiple Studies
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NEW
THIS YEAR!
Roundtable
Discussions |
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Topic 1: FDA 483 Warning Letters
Topic 2: How to Audit Effectively
Topic 3: In House vs. Outsourcing |
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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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