Mastering compliance and regulatory affairs

Highlights and presentations now available

Taking an in-depth look at compliance and regulatory affairs, this conference will help you discover innovative ways to improve cost-efficiency and shorten time to market.

Guest speakers from the life sciences industry will deliver a series of presentations, aimed at inspiring new ideas. Key topics will include improving knowledge sharing and data integration, reducing the risk and cost of litigation and security breaches, and meeting compliance and validation guidelines.

The conference will focus on current trends and strategic considerations and provide real-life examples of experiences with records, content and submission management.

Programme

Speakers

• Dr Stan Van Belkum, Programme Manager and Head of Information Processing, Medicines Evaluation Board, EMEA, Netherlands
  
• Per Helboe, Senior Director of Division, Danish Medicines Agency (Lægemiddelstyrelsen), Denmark
• Dr Joerg Stueben, Business Project Manager, IDEA for Controlled Documents, Boehringer Ingelheim, Germany
• Alastair J. Nixon, Director, Submission Publishing & Logistics, Global Regulatory Operations, GlaxoSmithKline, United Kingdom
• Andrew P Marr, Ph.D., EFPIA Topic Leader for PIM, United Kingdom
• Michael Sauter, Sr Director Global Reg Ops, Biogen Idec, United States
• Vincent Heenan, Director, Document Management Center of Excellence, Johnson & Johnson, United States
• Lars Johansson, Director of Scientific Information and Documentation, Bayer Schering Pharma AG, Germany
• Philip Dan Skou, Vice President, NNIT, Switzerland
• Joakim Kabongo, Records Management Specialist, NNIT, Denmark

Sponsors