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Research and Markets: Adverse Event Monitoring During Medical Device Clinical Trials - Post Conference Seminar (London)DUBLIN --(Business Wire)-- Research and Markets (http://www.researchandmarkets.com/research/38hdvl/adverse_event) has announced the addition of the "Adverse Event Monitoring During Medical Device Clinical Trials - Post Conference Seminar (London)" conference to their offering. The Adverse Event Monitoring During Medical Device Clinical Trials Post Conference seminar will be held on 31st January 2014 at The Rembrandt Hotel, London BENEFITS IN ATTENDING: This seminar provides a comprehensive overview of adverse event reporting issues during medical device clinical trials across Europe and i suitable for those with some experience of conducting medical device studies. The seminar will include case studies of different types of adverse events, highlight the different approaches across Europe and provide practical advice on how to manage these. PROGRAMME The Regulatory Requirements for Monitoring and Reporting Adverse Events How to Define and Classify Adverse Events Handling of Adverse Events During Clinical Investigations How to Design a Data Collection Form for Recording Adverse Events The Role of the Data Safety Monitoring Board The Role of the Competent Authority (CA (News - Alert)) Speakers: Janette Benaddi, CEO, Medvance Ltd Dates: 31 January 2014 Venue and Accommodation: The Rembrandt Hotel, 11 Thurloe Place, London SW7 2RS Directions: Opposite V&A Museum. Nearest underground station: South Kensington. For more information visit http://www.researchandmarkets.com/research/38hdvl/adverse_event About Research and Markets Research and Markets is the world's leading source for international market research reports and market data. We provide you with the latest data on international and regional markets, key industries, the top companies, new products and the latest trends. |
