This three-and-half-day, must-attend, education conference will use best practise case studies to explore current technologies, regulatory requirements and will provide delegates with techniques for the evaluation and implementation of cutting-edge technologies. In-depth discussion through four tracks will cover cost-effective, flexible, sustainable manufacturing facilities design and implementation; the use of IT and advanced technology in the drug manufacturing; drug supply and inspections requirements; and drug submissions and Quality by Design.Conference tracks will include:- Track 1: Managing Quality under the New Paradigm - Track 2: Regulatory Trends and Developments in Europe and Beyond - Track 3: Facilities of the Future Achieving Cost-Effective, Manufacturing, Flexibility - Track 4: IT Innovation for Effective Business Solutions and Regulatory ComplianceThe event will also feature an Executive Forum where key industry and regulatory experts will share information and insight on how to develop pharmaceutical operations model into a new transformational strategy that will deliver breakthrough performance.The sessions will be highly interactive combining examples of best practices both within the industry as well as from other relevant sectors, and latest updates and perspectives from regulatory authorities globally.