Mukul Krishna Global Director, Digital Media Frost & Sullivan Michele Cobham Submissions Manager, Regulatory Affairs Par Pharmaceutical Bernie Coney Senior Regulatory Specialist Pfizer Richard Brandt VP of Life Sciences Quark The FDA is mandating change faster than ever, but is the industry ready to rise to the challenge?  Technologies such as XML and semi-automated content approvals are at the fore-front of the new regulations.  The question is can the industry meet the new compliance requirements and, at the same time, actually yield cost-savings benefits in parallel business processes.   This live 60 minute complimentary eBroadcast will present the perspectives from both the industry and the vendor community about the challenges and the potential benefits of adopting new tools to rise above the compliance challenges.  Hear panel experts discuss the benefits of deploying dynamic publishing solutions to effectively comply with the FDA mandate while generating tangible benefits for the business process. During this eBroadcast, attendees will learn: New FDA regulatory requirements The technical challenges the requirements present How to meet regulatory change and leverage the approach throughout the organization and create a more efficient workflow  Click here to register and join industry experts from Frost & Sullivan, Par Pharmaceutical, Pfizer and Quark as they discuss how adopting an XML strategy to manage your content in-house not only provides you immediate value with regulatory compliance but also a differentiating business value in the long run. As our appreciation to you for joining us on this eBroadcast, all participants will be entered into a giveaway for a Kindle. All registrants will be eligible to receive a $500 credit voucher* toward any one of our upcoming Executive MindXchange events. * $500 Credit Voucher must be redeemed and allocated no later than Friday, December 4, 2009.