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November 29 - December 5, 2009

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Sat, Nov 21, 2009

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Sunday Nov 29	Monday Nov 30	Tuesday Dec 1	Wednesday Dec 2	Thursday Dec 3	Friday Dec 4	Saturday Dec 5
	MEDICAL DEVICE REGULATION IN ASIA PACIFIC Conference Clinical Trials Design for Medical Devices Course / Training / Workshop Preparation of FDA Submissions (INDs, BLAs, ANDAs, Post-Approval Supplements) and Communicating with the FDA Course / Training / Workshop Active Pharmaceutical Ingredient (API) and Drug Product Specifications Course / Training / Workshop Good Manufacturing Practices Course / Training / Workshop	MEDICAL DEVICE REGULATION IN ASIA PACIFIC Conference Clinical Trials Design for Medical Devices Course / Training / Workshop Preparation of FDA Submissions (INDs, BLAs, ANDAs, Post-Approval Supplements) and Communicating with the FDA Course / Training / Workshop Active Pharmaceutical Ingredient (API) and Drug Product Specifications Course / Training / Workshop Good Manufacturing Practices Course / Training / Workshop Selecting and Managing CROs Course / Training / Workshop	Cleantech Forum XXV- Beijing Conference Pharma partnering event PharmaVenue Conference Essentials of Clinical Study Management Course / Training / Workshop Active Pharmaceutical Ingredient (API) and Drug Product Specifications Course / Training / Workshop Good Manufacturing Practices Course / Training / Workshop Selecting and Managing CROs Course / Training / Workshop Technical Writing for the Pharmaceutical, Medical Device, and Biotech Industries Course / Training / Workshop CMC Regulatory Compliance for Biopharmaceuticals and Biologics Course / Training / Workshop	Pharma partnering event PharmaVenue Conference Best Practice in Phase IV Clinical & Observational Research Conference Dermatological Advances 2009 Conference Conference Essentials of Clinical Study Management Course / Training / Workshop RISK MANAGEMENT - Applying it and meeting the Challenges for Industry Course / Training / Workshop Technical Writing for the Pharmaceutical, Medical Device, and Biotech Industries Course / Training / Workshop CMC Regulatory Compliance for Biopharmaceuticals and Biologics Course / Training / Workshop Drug Master Files (DMFs) - Understanding and Meeting Your Regulatory and Processing Responsibilities Course / Training / Workshop How to Develop an Effective Complaint Handling and Post Market Surveillance Program for Drugs and Devices Course / Training / Workshop HOW TO WRITE SOPs Course / Training / Workshop 9:00am ADVANCED CLINICAL PROJECT MANAGEMENT - 2-Day workshop by HALLORAN Consulting Group Course / Training / Workshop	Best Practice in Phase IV Clinical & Observational Research Conference Dermatological Advances 2009 Conference Conference Essentials of Clinical Study Management Course / Training / Workshop Technical Writing for the Pharmaceutical, Medical Device, and Biotech Industries Course / Training / Workshop CMC Regulatory Compliance for Biopharmaceuticals and Biologics Course / Training / Workshop Drug Master Files (DMFs) - Understanding and Meeting Your Regulatory and Processing Responsibilities Course / Training / Workshop How to Develop an Effective Complaint Handling and Post Market Surveillance Program for Drugs and Devices Course / Training / Workshop CORRECTIVE AND PREVENTATIVE ACTION (CAPA) AND PROCESS IMPROVEMENT Course / Training / Workshop THE EU COSMETICS DIRECTIVE AND THE NEW COSMETICS REGULATIONS Course / Training / Workshop RISK MANAGEMENT - Applying it and meeting the Challenges for Industry Course / Training / Workshop 9:00am ADVANCED CLINICAL PROJECT MANAGEMENT - 2-Day workshop by HALLORAN Consulting Group Course / Training / Workshop

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