Advance Quality and Regulatory Symposium for the Biotech and Medical Devices Industry Conference (MQSS2011)
Venue: Radisson Warwick Plaza Hotel
|Event Date/Time: Apr 05, 2011||End Date/Time: Apr 06, 2011|
|Registration Date: Apr 06, 2011|
|Early Registration Date: Jan 31, 2011|
Hear directly from both present and former FDA experts on requirements that are becoming more rigorous in device manufacturing companies. Administer and take home best practices and practical approaches to compliance strategies that can be effectively implemented within your companyâ€™s daily processes. Discuss current risk-based approaches and understand what Investigators are really looking for and how to comply with emerging regulations, as well as which Quality System requirements are most scrutinized during inspection visits. This conference was designed to provide a comprehensive, cost effective compliance strategy for professionals in the drug, device and biologics industries. This two day event, is designed to provide attendees with a strong foundation for understanding the regulatory requirements of the US FDA as well as MDD/AIMDD. This course is designed to provide participants with an understanding of the current regulatory compliance issues cited in 483s and Warning letters, successful approaches to compliance, and meeting the concerns of regulators. Attendees will leave with a comprehensive set of tools for preparing regulatory initiatives, coping with challenges, and managing compliance.
Expert industry speakers and current and former FDA speakers address practical challenges and enforcement trends through informative and interactive sessions, and Panel discussions including a Questions and answer session.