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04-Mar-2010
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04-Mar-2010
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Fast Facts
Upcoming Conferences in California, United States RSS
For query: USA California
When Event Where
Mar-18-2010 Out-of-Specification Investigations – Beyond the laboratory Palo Alto, California United States
Mar-18-2010 Record Keeping for a food Recall: Keeping Records to Minimize the Affect of a Recall Palo Alto, California United States
Mar-18-2010 How to implement parametric release in EO sterilization-Practical approach Palo Alto, California United States
Mar-19-2010 Validating Radiation Sterilization for medical device industries Palo Alto, California United States
Mar-19-2010 Understanding Disinfectant Qualification Studies – How to avoid errors Palo Alto, California United States
Mar-23-2010 Planning for a Successful Pre-IDE Meeting with FDA Palo Alto, California United States
Mar-23-2010 Workforce Retention - Strategies for Strengthening Palo Alto, California United States
Mar-23-2010 Introduction to the safe use and storage of flammable liquids in laboratories and pharmaceutical manufacturing operations Palo Alto, California United States
Mar-23-2010 SOP Development for Medical Device Firms: Utilizing “lean compliance” principles to meet your quality system documentation requirements Palo Alto, California United States
Mar-24-2010 How to Create and Understand A Statistical Analysis Plan for A Clinical Study Palo Alto, California United States
Mar-24-2010 Overview of the Medical Device Risk Management Standard-ISO 14971 Palo Alto, California United States
Mar-24-2010 Clinical Evaluation Reports (CER's) Required for All Classes of Medical Devices in Europe Palo Alto, California United States
Mar-25-2010 Excel Spreadsheets - Develop and Validate to Eliminate 483s Palo Alto, California United States
Mar-26-2010 Calibration and Qualification in Analytical Laboratories Palo Alto, California United States
Mar-26-2010 Regulatory Requirements for Medical Device Calibration Programs Palo Alto, California United States
Mar-30-2010 The 2010 O\'Reilly Where 2.0 Conference San Francisco, California United States
Mar-30-2010 Document Approval, Control, and Distribution: How to Meet FDA QSR and ISO 13485 Requirements Palo Alto, California United States
Mar-30-2010 Effective Process Audit Discussion - A practical approach Palo Alto, California United States
Mar-30-2010 cGMP: Strategies for implementation and compliance for Phase I Investigational Drug and Biologic products Palo Alto, California United States
Mar-31-2010 Communicating to Staff-In a Down Economy Palo Alto, California United States
Mar-31-2010 ISO 13485:2003 for Medical Devices - How it differs to ISO 9001:2008 and FDA part 820 requirements Palo Alto, California United States
Mar-31-2010 21 CFR Part 11: Auditing for Part 11 Compliance Palo Alto, California United States
Apr-06-2010 Consumer Returns Roadshows 2010 San Jose, California United States
Apr-06-2010 Counseling and Discipline and Successful Outcomes Palo Alto, California United States
Apr-06-2010 International Financial Reporting Standards for SME’s Palo Alto, California United States
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